ML18152A257

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Insp Repts 50-280/94-26 & 50-281/94-26 on 940829-0902, 0907-12,27-28 & Via 940912 & 27 Telcons.Violations Noted. Major Areas Inspected:Licensee Radiation Protection Program, Specifically,High & Very High Radiation Areas
ML18152A257
Person / Time
Site: Surry  
Issue date: 10/12/1994
From: Rankin W, Wright F
NRC OFFICE OF INSPECTION & ENFORCEMENT (IE REGION II)
To:
Shared Package
ML18152A258 List:
References
50-280-94-26, 50-281-94-26, NUDOCS 9411030078
Download: ML18152A257 (17)


See also: IR 05000280/1994026

Text

UNITED STATES

NUCLEAR REGULATOAY COMMISSION .

REGION II

101 MARIETTA STREET, N.W., SUITE 2900

ATLANTA, GEORGIA 30323-0199

October 12, 1994

Report Nos. : 50-280/94-26 and 50-281/94-26

Licensee: Virginia Electric and Power Company

Docket Nos.:

50-280 and 50-281

License Nos.:

DPR-32 and DPR-37

Facility Name:

Surry 1 and 2

Inspection Conducted:

August 29 - September 2, September 7 - 12, and

.

.

Sept'::er 27 - 28'. 1994

Inso/Jctor:~})~ -:6-~

~

F. N. Wright

r--)

Approved by: r?..10-:::bZ \\( (. ~

W.

. Rankin, Chief

Facilities Radiation Protection Section

Radiological Protection and Emergency Preparedness Branch

Division of Radiation Safety and Safeguards

SUMMARY

Scope:

This routine, announced inspection of the licensee's Radiation Protection

(RP) program w~s made to review the implementation of the revised 10 CFR

Part 20 requirements.

The evaluation was made utilizing Temporary

Instruction 2515/123, "Implementation of the Revised 10 CFR Part 20." The

review focused primarily on the areas of: high and very high radiation areas;

Total Effective Dose Equivalent/As Low As Reasonably Achievable program

implementation; planned special exposures; and dose to the embryo/fetus for

declared pregnant woman.

Results:

Revisions to the RP program incorporating new requirements of 10 CFR Part 20

were made effective January 1, 1994.

The inspection included interviews with

licensee personnel, procedure and record reviews, and observations made during

tours of the licensee's radiological controlled areas.

The new requirements,

as focused by* the inspection procedure, were appropriately incorporated into

the RP program.

The inspector spoke favorably of the radiation protection

implementing procedures, which for the most part, appropriately addressed the

revised requirements and of the housekeeping in observed facilities.

One

violation was identified for failure to adhere to radiation protection

9411030078 941012

PDR

ADOCK 05000280

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PDR


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2

procedures for access to posted and controlled very high radiation areas

(Paragraph 3).

In addition, one non-cited violation.was identified

concerning the use of a checklist, for access into a posted and contrplled

very high radiation area, that was not procedurally controlled and approved

(Paragraph 3) .

I.

Persons Contacted

Licensee Employees

REPORT DETAILS

  1. M. Biron, Supervisor, Radiological Engineering

+*W. Benthall, Supervisor, Licensing

  • D. Boone, Quality Assurance

+#P. Cherry, Corporate Licensing

  • D. Christian, Station Manager

B. Dorsey, Supervisor, Exposure Control

  • D. Erickson, Superintendent, Radiation Protection

K. Ewell, Ftiel Handling Coordinator

  • A. Friedman, Superintendent of Nuclear*Training

+*B. Garber, Licensing

B. Hilt, Nuclear Training

  • J. McCarthy, Assistant Station Manager
  • D. Miller, Supervisor, Health Physics Operations
  • D. Nace, Radiological Engineering

M. Olin, Supervisor, Health Physics Technical Services

  • A. Price, Assistant Station Manager
  • R. Saunders, Vice President, Nuclear Operations

+D. Sommers, Licensing

D. Sweany, Training

  • B. Thornton, Corporate Health Physics

N; Urquhart, Supervisor, Nuclear Training, Radiological Protection

D. Whiti, Health Physics Shift Supervisor

Other licens~e employees contacted during the inspection included

technicians, maintenance personnel and administrative personnel.

Nuclear Regulatory Commission

  1. A. Belisle, Sectio~ Chief, Division of Reactor Projects, Region II
  • M. Branch, Senior Resident Inspector
  • D. Kern, Resident Inspector

+#W. Rankin, Facilities Radiation Protection Section Chief, Region II

  • D. Tamai, Resident Inspector
  • S. Tingen, Resident Inspector
  • D. Verrelli, Branch thief, Division of Reactor Projects, Region II
  • Attended September 2, 1994 Exit Meeting
  1. Participated in September 12, 1994 Teleconference

+Participated in September 27, 1994 Teleconference

Abbreviations used throughout this report are defined in the last

paragraph.

    • 2.

2

Preparation and Training for Implementation of the Revised 10 CFR

Part 20 Requirements {TI 2515/123). *

Training was reviewed to determine whether HP technicians, contractor HP

technicians and radiation workers were receiving appropriate

instructions concerning the revised 10 CFR Part 20 requirements for

their work assignments.

10 CFR 19.12 required that licensees instruct all individuals working or

frequenting any portion of the restricted areas in:

health protection

aspects associated with exposure to radioactive material or radiation;

precautions or procedures to minimize exposure;

purpose and function of

protection devices employed;

applicable provisions of the Commission

Regulations;

individuals responsibilities; and availability of

radiation exposure data.

The licensee's initial radiological protection NET training course was

required for all Virginia Power radiation workers prior to their

radiation work assignments at the station.

Prior to 1994, all radiation

workers were required to attend an abbreviated NET retraining class

annually.

In January of 1994, the licensee implementing changes to the

NET retraining program.

The new training plan only required licensee

radiation workers attend a classroom NET retraining session every three

years.

In the other years, licensee personnel were required to review

the NET Training Manual and certify their completion of the self-study

activities on a "Required Self-Study Receipt." Contract employee

radiation worker retraining requirements did not change and their

participation in an annual retraining class was required.

The 1993 NET

training programs for radiation workers provided the students with an

overview of the significant changes to the revised 10 CFR Part 20

requirements.

The inspector reviewed the instructor guides and the NET

Manual, Rev. 6, dated June 6, 1994.

The NET manual appropriately

addressed the, new terminology, revised dose limits, DPW policy, posting

of very high radiation areas, and PSEs.

However, neither the NET Manual

or the instructor guides addressed TEDE ALARA concept relative to work

in airborne radioactivity areas.

The inspector also determined that the

topic was not addressed in the NET test.

In interviews with the NET

instructors the inspector determined that the concept had. been addressed

in the classroom, even though the instructor guides did not specifically

list it as a topic of discussion or instruction.

In response to the

finding, the training department initiated a revision to the instructor

guides and developed a set of questions concerning the TEDE ALARA

concept.

The licensee was in the process of developing a computer based

training program for NET.

The inspector noted that the TEDE ALARA

concept was adequately addressed in the computer based retraining course

and that there was a TEDE ALARA problem for the students to demonstrate

their understanding of the topic.

In a limited number of interviews

with station employees the inspector did not identify a lack of

understanding concerning the TEDE ALARA concept.

In addition to

theformal introduction to the revised 10 CFR Part 20 requirements, the

licensee utilized other methods to provide the staff with information on

the revised requirements.

The licensee provided information on the

3

changes with the station video monitors, a continued source of

information for plant personnel. A pamphlet, "10 CFR 20 Revision,

Standards for Protection Against Radiation," outlining the significant

changes, was also provided to the staff.

The inspector reviewed the revised 10 CFR Part 20 training presented to

the site HPTs.

In 1992, the HPTCTPs for HPTs included a session related

to implementation of the revised 10 CFR Part 20 requirements.

Each

session was approximately 1 day in length and included reviews of

applicable regulations, comparisons of old and new regulations, licensee

policy and procedures for implementation of the requirements, and series

of questions and answers on the revised requirements.

The inspector

reviewed the following lesson plans:

0

0

0

HPTCTP-4-LP-54, "Orientation to the revised 10 CFR 20;"

HPTCTP-4-LP-55, "10 CFR 20 Update/Procedure Training;" and

_HPTCTP-4-LP-60, "Revised 10 CFR 20 (Dose Assignment)."

In 1993, the HPTCTP continuing training, rel~ted to the revisions to

10 CFR Part 20, concentrated on the application of the requirements in a

new series of draft radiological protection procedures.

The licensee

had previously established a Part 20 working group to prepare for the

implementation of the revised 10 CFR Part 20 requirements.

The working

group, made up.of representatives from Surry, North Anna and Corporate

Office, had been responsible for preparing SNSOC ready procedures in

draft form prior to the January 1, 1994, implementation date.

The draft

procedures were incorporated into the HPT continuing*training sessions

as they became available. The training process permitted the students

to become familiar with the revised requirements and the licensee's new

procedures for implementing those requirements. Student suggestions and

recommendations for the implementing procedures were also considered for

procedure improvements during the process.

The inspector reviewed the

following lesson plans utilized in 1993 HPTCTP:

0

HPTCTP-4-AG/APE-l, "Special Training Radioactivity Effluent

Monitoring Program Draft Procedures Developed to Implement the

0

HPTCTP-3-AG-6, "Use of H.P. Draft Procedures - 1032.XXX Series;"

0

HPTCTP-3-AG/APE-8, "Task Training Completion of NRC Forms 4 and

5; II .

0

HPTCTP-3-AG/APE-10, "Task Training Manipulating PREMS;"

0

HPTCTP-4-LP-68, "Special Training Review of HP Draft Procedures

1032.050, 1042.XXX, and 1081.010 Series;"

0

HPTCTP-4LP-69, "Special Training Internal Dose/Bioassay Program

IAW HP-1041.XXX Draft A Procedures;"

0

HPTCTP-4-LP-70, "Special Training Procedure Changes/Industry

Events;" and

0

HPTCTP-6-TS-5, "HP-1061.021, Draft A Contaminated Skin Dose

Assessment."

3 .

4

The licensee conducted the following HPTCPT training in 1994:

0

HPTCTP-6-TS-6, "10 CFR 20 Revisions - Radiological Protection,"

and

0

HPTCTP-4-72-DRR, "IO CFR 20 Following Implementation."

The traitiing provided the student a review* of the significant changes

resulting from the implementation of the revised requirements, and

provided an opportunity for the HPTs to identify strengths and/or

weaknesses in the radiological protection program areas impacted by the

revised requirements.

The inspector reviewed the licensee's lesson plans for contract HPTs and

determined that the training included a review of the licensee's

procedures incorporating the changes of the revised 10 CFR Part 20

requirements prior to their HP work assignment.

In general, the training programs for radiation workers and HPTs

included sufficient instructions concerning revisions to 10 CFR Part 20

and appeared appropriate for the students needs.

No violations or deviations were identified.

High and Very High Radiation Areas (Tl 2515/123)

This area was reviewed to evaluate the licensee's implementation of

r.equirements specified for the control ,of HRA and VHRA as prescribed in

Paragraphs 20.1601 and 20.1602 of 10 CFR Part 20, "Subpart G-Control of

Exposure from External Sources in Restricted Areas."

Paragraph 20.1601, "Control of Access to High Radiation Areas," states

in part (a);

"The licensee shall ensure that each entrance or access

point to a HRA have one or more of the following features:

(3)

Entryways that are locked, except during periods when access to the

areas is required, with positive control over each individual entry."

Paragraph 20.1602, "Control of Access to Very High Radiation Areas,"

states; "In addition to the requirements in 20.1601, the l~censee shall

institute additional measures to ensure that an individual is not able

to gain unauthorized or inadvertent access to areas in which radiation

levels could be encountered at 500 rads or more in 1 hour1.157407e-5 days <br />2.777778e-4 hours <br />1.653439e-6 weeks <br />3.805e-7 months <br /> at 1 meter

from a radiation source or any surface through which the radiation

penetrates."

Paragraph 20.1101, "Radiation Protection Programs," (a) states; "Each

licensee shall develop, document, -and implement a radiation protection

program commensurate with the scope and extent of licensed activities

and sufficient to ensure compliance with the provisions of this part."

TS 6.4.B states procedures for personnel radiation protection shall be

prepared consistent with the requirements of 10 CFR Part 20 and shall be

approved, maintained and adhered to for all operations involving

personnel radiation exposure.

5

Paragraph 20.1601.(c) provided a licensee may apply to the Commission

for approval of alternative methods for controlling access to HRAs.

The

licensee's alternative control measures for entry into HRAs were

described in the licensee's TS.

Licensee TS 6.4.8.1 states, in part, "In lieu of the "control device" or

"alarm signal" required by paragraph 20.1601 of 10 CFR 20, each high

radiation area in which the intensity of radiation is greater than

100 mrem/hr but less than 1,000 mrem/hr shall be barricaded and

conspicuously posted as a high radiation area and entrance thereto shall

be controlled by requiring issuance of a Radiation Work Permi_t." A

footnote,to this TS requirement related to the use of RWPs was:

"Health Physics personnel shall be exempt from the RWP issuance

requirement during the performance of their assigned radiation

protection duties, provided they comply with approved plant radiation

protection procedures for entry into high radiation areas."

In addition, any individual or group of individuals permitted to enter

such areas were to be provided with one or more of the following:

0

A radiation monitoring device which continuously indicated the

radiation dose rate in the area;

0

A radiation monitoring device which continuously integrated the

radiation dose rate in the area and alarmed when a preset

integrated dose was received; or

0

An individual quali.fied in radiation protection procedures who was-

equipped with a radiation dose rate monitoring device, responsible

for providing positive control over activities within the area and

made periodic radiological surveys as specified by HP in a RWP.

In addition to the requirements of TS 6.4.8.1, Paragraph 6.4.8.2

required:

0

Areas assessable to personnel with the intensity of radiation was

greater than 1,000 mrem/hr, but less than 500 rads/hr at one meter

from a radiation source or any surface through which radiation

penetrates shall be provided with locked doors to prevent

unauthorized entry; and

~

Keys shall be maintained under the administrative control of the

Shift Supervisor on duty and/or the senior station individual

assigned responsibility for radiation protection.

VPAP-2101, "Radiation Protection Program," Rev. 6, dated July 28, 1994,

established Virginia Power's Radiation Protection Plan, which set forth

the requirements of the Radiation Protection Program for Surry and

North Anna.

Section 5.2, of VPAP-2101, stated in part, "Station

Radiological Protection Department is responsible for ensuring

procedures, personnel, and other resources are established to implement

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6

the Station Radiation Protection Program."

The inspector reviewed .the

following licensee procedures for posting, entry requirements and key

controls for HRAs:

0 .

HP-1081.10, "Radiation Work Permits: Preparing and Approving,!'

Rev. 5, dated, January 24, 1994, provided instructions for Shift

Supervisors Health Physics and RWP Writers to prepare and approve

RWPs as required by VPAP-2101.

0

HP-1032.060, "Radiological Posting and Access Control," Rev. 0,

dated December 7, 1993, provided instructions for posting

radiological areas and implementing access controls.

0

HP-1032.061, "High Radiation Area Key Control," Rev. Ot dated

December 7, 1994, provided instructions to HP Operations for

verifying entry requirements, determining key type, issuing and

accounting for keys to locked HRAs.

The licensee's radiation protection plan, VPAP-2101 made the following

distinctions for HRAs:

0

HRA - Areas accessible to personnel, having a whole body dose rate

in exce*ss of 100 mrem/hr, 30 centimeters from the source;

0

HRA Exceeding 15 Rem/hr - High radiation areas accessible to

personnel, having a whole body dose rate greater than

15,000 mrem/hr, 30 centimeters from the source; and

0

VHRA - Areas accessible to personnel, having a dose rate exceeding

500 rads/hr, 1 meter from the source.

TS 6.4.B.2 required areas with the intensity of radiation greater than

1,-000 mrem/hr, but 1 ess than 500 rads/hr at one meter from source, be

locked to prevent unauthorized entry into such areas and the keys shall

be maintained under _the control of the Shift Supervisor on duty and/or

the senior station individual assigned the responsibility for health

physics and radiation protection.

The inspector reviewed the licensee's HRA key controls with licensee

representatives and determined that the HP Shift Supervisor maintained a

HRA key cabinet and check-out logbook for the control of HRA keys.

The

keys to locked HRA and HRAs exceeding 15 rem/hr were maintained in a key

cabinet on a wall in the HP work area. Licensee personnel reported that

there were only two plant areas that were posted and controlled as

VHRAs, the Unit 1 and Unit 2 Incore Sump Rooms in the Reactor

Containment Buildings.

The licensee controlled the Incore Sump Room as

a VHRAs due to the potential and significant radiological hazards to

personnel associated with the withdrawal of incore detectors from the

core into the Incore Sump Room.

licensee personnel pointed out that the

radiation lev~ls in the Incore Sump Room were usually less than

  • e

~-------=--------:::--=-_-~ -

7

100 mrem/hr and had not met the definition of a VHRA (500 rads/hr)

during any of the recent entries made into the rooms.

During the review

of the HRA key issuance log, the inspector noted that the logbook did

not contain a copy of Attachment 4, "Very High Radiation Area Key Log,"

of HP-1032.061.

When the inspector inquired about the key issue to the

Incore Sump Rooms lic~nsee personnel made available two foldets out of

the Health Physics Operations Managers office.* Each folder contained a

log of key issuance to the Incore Sump Room, some copies of RWPs, "CL-10

Incore Sump Room Entry" forms and the keys for the locks securing access

to the Incore Sump Rooms.

The key issues were documented on "Incore

Instrumentation Sump Room - Key Control Log" forms that were not

controlled or described by the licensee's procedures. The*Unit 1 folder

showed keys to the Unit 1 Incore Sump Roo~ had been issued approximately

17 times in the period of January 27, 1994 through March 23, 1994.

The

Unit 2 folder showed that keys to the Unit 2 lncore Sump Room had been

issued approximately 6 times during the period of June 6, 1994 and

June 18 1994.

The inspector reported to licensee personnel, that the key issuance did

not appear to have been made in accordance with the requirements of

HP-1032.061 and requested copies of the material in the two folders and

recent radiological surveys of the areas for further review.

The

inspector also reported that all of the RWPs in the folders did not

appear to have been SNSOC approved as required.by VPAP-2101,

Section 6.3.12. The inspector noted that the staff did not appear

familiar with the requirement.

The licensee provided the additional

documentation to the inspector that afternoon.* That evening the

inspector determined that, of the documentation provided at that time,

only 2 of 5 RWPs found in the licensee's 1ncore Sump Room folders had

actually received SNSOC approval, as required by the Radiation

Protection Plan for entries into a posted and controlled VHRA area.

Additionally, the keys were not issued and documented in accordance with

the requirements of licensee procedure HP-1032.061, for any of the

23 key issues to the Incore Sump Room.

The inspector also determined

that a checklist, "Incore Sump Room Entry Checklist" utilized to provide

1 and document certain radiological protection controls for issuing keys

and granting access into the Unit 1 and 2 Incore Sump Rooms was not

addressed in radiation protection procedures and was not procedurally

controlled and approved.

The following morning, and just prior to the exit meeting, the inspector

reported to the Superintendent of Radiation Protection that:

1) There

appeared to be violations related to failure to follow procedures for

HRA access and key controls; and 2) A violation for the use of a

checklist, utilized in preparations for access and radiological controls

into a posted and controlled very high radiation area, that was not

controlled by written and approved procedures.

The inspector reported

the extent of the problem (number of violations) could not be made at

that time, in that, the inspector did not have*all of the licensee's

documentation concerning all of the 1994 entries into the Incore Sump

Rooms.

The inspector requested copies of documentation showing the

8

"Tag-Out" of the incore detectors during Incore Sump Room entries, all.

_ RWPs utilized in access to the In core Sump Rooms and the CL-10 forms

completed for each entry. At the NRC inspection exit meeting, the

inspector reported that there were examples of procedure violations, as

described above, and that the findings would remain an unresolved item

pending a review of additional documents the RP staff had previously

agreed to provide to the inspector in the following week.

The inspector

received the information on September 7, 1994.

The additional

information provided to the inspector included documentation of Incore

Detector "Tag-outs", copies of all RWPs utilized in accessing the Incore

Sump Room, RWP Briefing Attendance Sheets and the identification of the

RWP that was uti_l ized by the personnel assigned a key to the Incore Sump

Room.

The licensee also reported that one key issuance indicated in the

licensee's logbook had not been made, reducing the number of key issues

and entries into the Unit 1 Incore Sump Room to 16 and the total number

of entries into the Unit 1 and 2 Incore Sump Rooms to 22 for 1994.

The

licensee indicated the issue correction on the log-sheet following the

inspectors request of the documentation.

Following the review of the submitted documentation, the inspector

determined that there were several examples of failure to adhere to'

written, controlled, and approved procedures for access to the Incore

Sump Room.

The findings were discussed with licensee representatives in*

a teleconference on September 12, 1994.

The findings included the

following:

0

In 1994, keys to the Unit 1 or Unit 2 Incore Sump Room were issued

to personne 1 ut il i zing 7 different RWPs.

Of the 7 RWPs ut il i zed

  • only 4 RWPs specifically included the Incore Sump Room as a work

location (94-2-2076, 94-2-2047-(Rev. 5 only}, 94-2-2090 and 94-2-

3097}.

Section 6.8 of VPAP-2101 stated that the primary method of

controlling work that involved radiological hazards was the RWP

system.

Section 6.8.7.d stated, workers, before start of work

shall read applicable RWP and ask questions about any part of the

RWP that they do not understand. Section 5.11 of VPAP-2101

required Station personnel be responsible for conducting work with

a high level of performance in radiological protection including

following posted, written and RP verbal radiological instructions.

Section 6.3.1 stated, in part, that if a worker was to enter a

posted HRA, it was the worker's responsibility to verify he or she

was authorized by an RWP to enter the area.

In 1994, six of

twenty-two personnel entries into the Incore Sump Rooms, posted

and controlled very high radiation area, were made with a RWP that

did not address the licensee's controls and requirements for entry

into the Incore Sump Rooms.

Two of the RWPs, 94-2-2001 and 94-2-

3001, utilized by four licensee personnel to enter into the Incore

Sump Room specifically excluded the Incore Sump Room as a work

location for those RWPs.

The inspector reported that failure of

six radiation workers, assigned keys to controlled VHRAs, to enter

the Incore Sump Rooms, on the correct RWP as required by VPAP-

2101, was a violation of TS 6.4.B requirements for failure to

adhere to radiation control procedures. *

~~-

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9

VIO 50-280, 281/94-26-01:

FIRST EXAMPLE:

Failure of six

radiation workers to follow procedures and utilize the appropriate

RWP for access into a posted and controlled VHRA.

0

Procedure step 6.3.12.c. of Section 6.3.12, "Access Controls for

Very High Radiation Areas," of VPAP-2101, required "Specific SNSOC

approval shall be required for planned entry into the area." The

inspector determined that during the period of January through

June 1994, the licensee failed to obtain SNSOC approval for RWPs

94-2-2076, 94-2-2047 (Rev. 5}, and 94-2-2090 utilized for entry

into posted and controlled very high radiation areas.

The

inspector stated that failure to obtain SNSOC approval for RWPs

controlling access to the Incore Sump Rooms was a violation of

TS 6.4.B. requirements for failure to adhere to radiation control

procedures.

SECOND EXAMPLE:

Failure to follow radiation control procedures

requiring SNSOC approval for three RWPs utilized to control work

in the Incore Sump Room, a posted and controlled VHRAs.

0

Step 6.4.2 of licensee procedure HP-1032.061, "High Radiation Area

Key Control," Rev. O, dated December 7, 1994, required persons

receiving a key for access into VHRA review the requirements of

Attachment 1, "Requirements and Responsibilities To Enter A Locked

High Radiation Area." Attachment 4, "Very high Radiation Area Key

Log," of 1032.061 provided the licensee with documentation of the

"responsibi.l ity review" by signature when the keys were issued.

Step 6.4.3, required the following information be recorded on

Attachment 4, RWP number applicable to entry; gates or areas to

be entered or key to be used; key requester printed name,

signature, and TLD badge number;

Health Physics coverage

technician printed name, signature, and badge number; key issue

date and time; initials of person issuing the key, and remarks.

The inspector determined that during the period of January 27

through June 18, 1994, the licensee failed to.adhere to radiation

control procedure HP-1032.061 and document the "responsibility

reviews," and other information required by Attachment 4, for all

(22} key issues to the Unit 1 and 2 Incore Sump Rooms, posted and

controlled VHRAs.

The inspector stated that failure to document

the "responsibility reviews," and other information required by

Attachment 4 for key issues into the Incore Sump Rooms was a

violation of TS 6.4.B., "Requirements for failure to adhere to

radiation control procedures."

THIRD EXAMPLE:

Failure to issue keys to a posted and controlled

VHRA in accordance with licensee procedure HP-1032.061.

Various operating and maintenance procedures for the Incore Detectors

required the user to notify Health Physics prior to movement or

maintenance of the detectors and to require "tag-out" of the detectors

during periods when personnel access into containment buildings was

permitted.

The inspector determined that the incore detectors had been

10

made inoperable, using a "tag-out" procedure, throughout all periods

when entries into the Incore Sump Room were made in 1994.

The Health Physics staff was utilizing an "Incore Sump Room Entry"

checkl,ist, commonly referred to as "CL-10" to prepare for entries into

the Incore Sump Rooms.

The checklist was used to ensure certain

radiological protection measures and controls were made prior to

granting access and issuance of keys to the Unit 1 and 2 Incore Sump

Rooms.

The CL-10 checklist documented:

Approval of HP Operations

Supervisor to enter the area; HP Operations verification that detectors

were not exposed and the detector drive systems had been "tagged out;"

radiological survey requirements; and key issuance for access to the

areas.

However, the inspector determined that the use of the CL-10

checklist was not described or procedurally controlled and approved.

The inspector stated that the use df the CL-10 checklist was a violation

of TS 6.4.B. requirements, in that, it was a procedure utilized by the

licensee for certain radiological protection measures that was' not

procedurally controlled or approved.

Licensee corrective action for the

violation included incorporating the "CL-10 Incore Sump Room Entry"

checklist into a higher tier litensee procedure, HP Procedure 1032.061.

This NRC identified viol~tion is not being cited because criteria

specified in Section VII.B of the Enforcement Policy were satisfied.

NCV 50-280, 281/94-26-02: Violation of Technical Specification 6.4.B

requirements for use of a procedure that was not controlled and

approved.

The safety significance of the violations was low due to the fact that

the Incore Sump Room did not have entries with dose rates in excess of 1

rem/hr.

However, the numerous examples of individuals failing to comply

with radiation protection procedures indicated the need to re-evaluate

the adequacy of existing access control procedures and/or staff

awareness of those procedures to ensure the procedures were controlled

and implemented.

-

During tours of the plant, the inspector noted that the licensee's

posting and control of radiation areas, HRAs, contamination areas, and

radioactive material areas were generally adequate. All HRAs were

locked as required.

No deviations were identified.

4.

Declared Pregnant Women and Embryo/Fetus Doses (TI 2515/123)

This program area was reviewed to determine that the licensee's program

for DPW met the regulatory requirements and that doses to the

embryo/fetus were within the regulatory limits.

The licensee's DPW policy was clearly described in VPAP-2101.

The

definition of a DPW was provided in Section 4.0, "Definitions" and the

licensee's dose limits for a DPW were specified in Section 6.3.2 which

11

agreed with the limits of 10 CFR 20.1208(a) and (d). The licensee's

procedures permitted workers three options including:

1.

Elect to declare pregnancy, become a DPW, and work within

the regulatory and administrative embryo/fetus dose limits;

2.

Elect not to declare pregnancy, not be a DPW, and work

within occupational dose limits; and

3.

Elect to withdraw DPW status, no longer be a DPW and return

to work within occupational dose limits.

VPAP-2101 clearly stated that the choice to declare or not to declare

pregnancy was strictly voluntary, a DPW may choose any of the options

  • and could withdraw her declaration at any time.

HP-1031.020,

Administrative Dose Control, Rev. 0, dated December 7, 1993, reflected

the DPW program requirements of VPAP-2101.

Section 6.3.5, of VPAP-2101 described the licensee's administrative dose

control for DPW's.

The Exposure Control staff initially set the DPW

dose limit to zero to prevent a DPW from obtaining dosimetry and

entering the RCA prior to an embryo/fetus dose determination.

The

Exposure Control group performed WBCs and determined any internal dose

to embryo/fetus, determined external dose and with an estimated date of

conception estimated TEDE dose to the embryo/fetus.

Licensee procedure

HP-1041.024, "Embryo/Fetus Dose: Internal Dose Calculation" provided

instructions for calculating embryo/fetus dose due to internal

radionuclides in DPW at time of conception and due tri intakes of

radionuclides during pregnancy.

NRC Regulatory Guide 8.36, "Radiation

dose to the Embryo/Fetus provided the basis for the procedure.

If the

embryo/fetus dose exceeded 450 mrem the DPW was restricted from access

to the RCA.

If the TEDE dose to the embryo was less than 450 mrem the

licensee permitted a dose extension up to 450 mrem with efforts to limit

monthly embryo/fetus TEDE dose to 50 mrem/month.

Section 6.3.5 also

described measures to take when an individual withdrew voluntary DPW.

The inspector requested a list of individuals that had declared DPW and

attempted t6 review the individuals personnel exposure records,

maintained by the Records Department, to determine that "Voluntary

Declaration of Pregnancy" and embryo/fetus dose determination documents

were maintained as required by on 10 CFR 20.2106(e).

The inspector was

unable to find most of the required DPW documents in the individual's

exposure record files. The finding was reported to licensee management

and the licensee was able*to find the applicable documents the following

day.

Licensee representatives reported that the records had been sent

to Records Department but had not been filed in the exposure files when

they were requested by the inspector. The inspector reported a review

of the deposition of personnel dosimetry records would be made in a

future inspection as an IFI.

IFI 50-280,281/94-26-03:

Review licensee's procedures and program for

personnel exposure record maintenance.

12

During the inspection, the inspector interviewed several female

employees concerning the licensee's program for DPWs.

Through those

discussions the employees appeared to be knowledgeable of the licensee's

requirements in this area and reported the declaration was voluntary.

The inspector determined that, in general, the licensee had established

adequate policies and procedures for implementing the requirement of

10 CFR 20.1208, "Dose to an Embryo/Fetus."

The licensee DPW dose

assessments were appropriate and dose was within limits. The licensee's

- policy for DPWs, as demonstrated by its implementation, appeared to be

equitable and ALARA.

No violations or deviations were identified.

5.

TEDE ALARA and Respiratory Protection (TI 2515/123)

This area was reviewed to determine whether the licensee had established

an adequate training program, policy, and procedures to maintain worker

TEDE ALARA while performing work in airborne radioactive material areas.

10 CFR 20.llOl(b) required that the licensee use, to the extent

practicable, procedures and engineering controls based upon sound

radiation protection principles to achieve occupational doses and doses

to members of the public that are ALARA.

The inspector reviewed the following licensee procedures:

0

VPAP-2.102, "Station ALARA Program," Rev. 2, dated December 6,

1994;

0

HPAP-1042, "Respiratory Protection Program," Rev. 1, dated

December 12, 1994;

0

HP-1081.10, Radiation Work Permits: Preparing and Approving,

Rev .. 5, dated-January 21, 1994; and

0

HP-1042.210, "Respiratory Hazards Evaluation and Respiratory

protection Selection," Rev. O, dated December 6, 1993.

Section 6.4.7, "Respiratory Protection - Policy Regarding. Respirators,"

of VPAP-2101, incorporated the TEDE ALARA concept, to maintain TEDE

ALARA while working in airborne radioactivity areas, in the respiratory

protection program objectives. The licensee's respiratory protection

program policy stated actual and potential sources of airborne

radioactivity during routine operations should be identified and proper

engineering controls implemented.

The policy also stated that when

activities were conducted infrequently or were non-routine and the use

of engineering controls are impractical the use of respirators to avoid

excessive exposure to airborne radioactivity was appropriate, while

maintaining TEDE ALARA.

.

VPAP-2102, Station ALARA Program, required an ALARA TEDE Evaluation if

one or more of the following conditions wa~ met:

13

0

Individual estimated DDE for a RWP job while using respirator will

exceed 0.5 rem;.

0

Ratio of DDE dose rate, mrem/hr, to DAG fraction is greater than

50 and, without respirator use, individual DAG-Hour exposure would

exceed 10 DAG-Hours; or

0

Selected respirator PF is less than expected peak DAG fraction and

respirator is to be used to limit intake.

The licensee documented TEDE ALARA reviews using Attachment 21, ."TEDE*

ALARA Evaluation-720134 (Jan 94)." of VPAP-2102.

Through discussions with licensee representatives, the inspector

determined that the licensee had continued to reduced the use of

respirators in various activities. in recent years. Licensee

representatives reported that the reduction in use of respirators had

resulted in some personnel contaminations. A summary of the respirator

use, annual site dose, and PGEs are showed below.

The figures show.

increases in the number of personnel contaminations with the reductions

in respirator usage from 1993 through 1994; however, *there were no

significant doses resulting from the contaminations.

The licensee

reported that there were a total of 115 positive WBGs during the period

of January 1 through May 10, 1994. There were 3 individuals with a dose

in the range of 10-12 mrem, these were the most significant.

Approximately one third were less than 2 mrem.

The dose following 1992

also shows decline while the RTD removal projects were completed in 1992

anti 1993.

YEAR

91

92

93

94

NO. RESPs

9,234

10,461

2,276

368

ANNUAL

SITE.

DOSE (REMS)

509

538

387

293

PGEs

124

122

99

169 (Through *

September 2,

1994)

TEDE ALARA training is addressed in Paragraph 2 of.the report. The

inspector determined that the licensee had made efforts to maintain TEDE

exposures ALARA, while working in airborne .radioactive material areas.

No violations or deviations were identified.

6.

Planned Special Exposures (TI 2515/123)

This area was reviewed to determined whether the licensee's program for

PSEs met the regulatory requirements.

10 GFR 20.1206 permits the licensee to authorize an adult worker.to

receive doses in addition to and accounted for separately from the doses

received under the lim1ts specified in 10 GFR 20.1201 provided that

certain conditions are satisfied. Such exposures cannot exceed the dose

,.........----

~-

- -

--- -

- -- -

.-

7.

14

limits in 10 CFR 20.120l(a) in any year or five times the annual dose

limits during an individual's lifetime.

Section 6.3.13, "Dose Controls for Planned Special Exposures," of VPAP-

2101, described the licensee's policy and requirements for PSEs.

The

policy states:

"~SEs shall be authorized only in an exceptional situation, when

alternatives that might avoid the higher exposure are unavailable or

impractical.

Dose received in excess of annual limits, including doses

received during accidents, emergencies, and PSEs must be subtracted from

the limits for PSEs that the individual may receive during the current

year and during the individual's lifetime."

VPAP-2101 described the* administrative controls to initiate a PSE and

adequately addressed the requirements of 10 CFR 20.1206.

The procedure

required a PSE be documented and approved in writing prior to allowing

the exprisure to be received.

The _approval list included:

Worker~

Department Superintendent, Workers Employer Representative (if non-_

Virginia Power employee), Superintendent of Radiological Protection,

Station Manager or Assistant Station Manager, and the Vice President-

Nuclear Operations or the Assistant Vice President Nuclear Operations.

Through discussions with licensee representatives and a review of

records, the inspector determined that the licensee had appropriate

procedural guidance for allowing PSEs.

The inspector determined that

the licensee had not authorized any PSEs.

No violations or deviations were identified.

Exit Meeting (TI 2515/123)

The inspection scope and findings were summarized on September 2, 1994,

with those persons indicated in Paragraph 1.

The inspector described

the areas inspected and discussed in detail the inspection results. The

inspector reported that there appeared to be radiation protection

procedure violations concerning failure to follow procedures and use of

a checklist that was not procedurally controlled and approved.

Dissenting comments were not received from the licensee. The licensee

did not identify any documents or processes as being proprietary.

On

September 12, 1994, a teleconference was made ~ith the persons indicated

in paragraph 1 to discuss the inspectors findings following licensee'~

submittal of additional documentation associated with Incore Sump Room

entries in 1994.

At that time, the inspector reported the inspection

results listed below.

Another teleconference was requested by the

licensee and held September 27, 1994.

The licensee pointed out that

there were procedural controls for controlling movement of incore

detectors in the incore detector operating and maintenance procedures

and the licensee submitted copies of procedures indicating those_

controls.

However, that information was previously recognized by the

inspector and did not affect the findings shown below .

15

IYQg Item Number

Status

Description and Reference

VIO

50-280, 281/94-26-01

Open

Failure to follow procedures,

three examples. (Paragraph 3) .

NCV

50-280, 281/94-26-02

Closed

Failure to control and approve

procedure (Paragraph 3).

IFI

50-280, 281/94-26-03

Open

Review licensee processing and

document control of personnel *

dosimetry records

(Paragraph 4).

8.

Index of Abbreviations Used in this Report

ALARA

CFR

DAC

DPW

HEPA

HPT

HPTCTP

HRA

IFI

IR

mrad

mrem

NET

NRC

PCE

PF

PREMS

PSE

RCA

REV

RM

RP

RTD

RWP

SNSOC

TEDE

TI

TLD

TS

VHRA

VIO

VPAP

WBC

As Low As Reasonably Achievable

Code of Federal Regulations

Derived Air Concentration

Declared Pregnant Woman

High Efficiency Particulate Air-filter

Health Physics Technician

Health Physics Technician Continuing Training Program

High Radiation Area

Inspector Followup Item

Inspection Report

Milli-Radiation Absorbed Dose

Milli-Roentgen Equivalent Man

Nuclear Employee Training

Nuclear Regulatory Commission

Personal Contamination Event

Protection Factor

Personnel Radiation Exposure Management System

Planned Special Exposure

Radiation Control Area

Revision

Radioactive Material

Radiation Protection

Resistive Temperature Detector

Radiation Work Permit

Station Nuclear Safety and Operating Committee

Total Effective Dose Equivalent

Temporary Instruction

Thermoluminescent Dosimeter

Technical Specifications

Very High Radiation Area

Violation

Virginia Power Administrative Procedure

Whole Body Counting