ML17284A610

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Insp Rept 50-397/88-36 on 881010-14.Violations Noted. Major Areas Inspected:Organization & Mgt Controls,Followup, Facilities & Equipment & Tours of Facility
ML17284A610
Person / Time
Site: Columbia 
Issue date: 11/03/1988
From: Cicotte G, North H
NRC OFFICE OF INSPECTION & ENFORCEMENT (IE REGION V)
To:
Shared Package
ML17284A608 List:
References
50-397-88-36, NUDOCS 8811210195
Download: ML17284A610 (14)


See also: IR 05000397/1988036

Text

U.

S.

NUCLEAR REGULATORY COMMISSION

REGION

V

Report

No. 50-397/88-36

Docket No. 50-397

License

No.

NPF-21

Licensee:

Washington Public Power

Supply System

P.

0.

Box 968

Richland,

Washing

on

99352

Facility Name:

Washington

Nuclear Project

No.

2

Inspection at:

WNP-2 Site,

Benton County, Washington

Inspection

Conducted:

October 10-14,

1988

Inspector

Approved by

G.

R. Cicott

, Radiation Specialist

H.

S. North, Acting Chief

Facilities Radiological Protection Section

/l 9

PP

Date Signed

ZP

Da e Signed

~Summa r:

Ins ection durin

eriod of October 10-14

1988

Re ort No. 50-397/88-36

Areas Ins ected:

Routine,

unannounced

inspection

by a regionally based

inspector of organization

and management

controls,

followup, facilities and

equipment,

and tours of the facility.

Inspection procedures

30703,

83722,

92701,

83727,

and 83726 were addressed.

Results:Of the four areas

addressed,

no violations were identified in three

areas.

In one area,

a violation of'0

CFR 20.203

was identified, involving a

radiation area which was not posted (report section 5).

An unresolved

item,

regarding documentation

and control of radioactive material

storage

areas,

was

. identified (report section 4).

The licensee's

program appeared

capable of

meeting its safety objectives.

DETAILS

1.

Persons

Contacted

"G.

C.

"J.

W.

R. J.

~T.

M.

A. I.

W.

S.

R.

G.

AD

D.

A.

E

"R.

L.

"M.

R.

Sorensen,

Manager,

Regulatory

Programs.

Baker, Assistant Plant Manager

Barbee,

Plant Engineering Supervisor

Bradford, Health Physics

Supervisor

Brun, Plant guality Assurance

Engineer

Davis, Senior Radiochemist

Davison,

Compliance

Engineer

Graybeal,

Health Physics/Chemistry

Manager

Larson, Radiological

Programs/Instrument

Calibration Manager

Pisarcik,

ALARA Supervisor

Shockley,

Health Physics

Support Supervisor

Wardlow, Health Physicist

Wuestefeld,

Assistant Plant Technical

Manager

In addition to the individuals identified above,

the inspector

met and

held discussions

with other members of the licensee's

staff and

personnel.

"Denotes

those present at the exit interview held on October 14,

1988.

2.

Or anization

and

Mana ement Controls

A.

~Staffin

The licensee

stated that two additional

Health Physics

(HP)/Chemistry personnel

were being hired to reduce

the backlog of

work requiring

HP coverage.

Additionally, the licensee

had two

contractor

HP Technicians

(HPTs)

on site.

Some licensee

HPTs stated

that many lower priority tasks

were being deferred

due to staffing

limitations.

Identification and Correction of Weaknesses

The licensee

had recently instituted several

changes

to their

problem identification process.

When

a problem with a high

radiation area enclosure

lock mechanism

was identified (see

paragraph

5, below), the licensee

immediately held a meeting to

investigate

the problem, which was quickly resolved.

Non-Conformance

Reports

(NCRs), Radiological

Occurrence

Reports

(RORs),

and Personnel

Contamination

Reports

(PCRs)

from June

15 to

October 10, 1988,

were reviewed to evaluate

the effectiveness

of the

licensee

s program.

Two incidents

reported in RORs, involving

multiple personnel

contaminations

and an administrative

overexposure,

would typically have resulted in initiation of NCRs,

under the discretionary authority of the

HP Supervisor.

In both

cases,

an investigation of sufficient depth to meet the intent of

the procedures

had been

conducted.

The

HP Supervisor stated that

NCRs would be completed in order to document the review that had

taken place.

Licensee

Procedure

PPM 11.2. 19. 1, Investi ations of Non-Re ortable

Radiolo ical Occurrences,

Revision 7, dated 09/07/88,

was reviewed.

The purpose of the procedure

was described

as the reporting of

'vents

not deemed to have resulted in non-compliance with regulatory

requirements.

Among the criteria listed for matters warranting

initiation of a Report of Radiological

Occurrence

(ROR) was

"suspected

radiation overexposure"

~

The licensee's

philosophy

concerning the use of RORs

and

NCRs was discussed

with the

HP

Supervisor

and with the Health Physics/Chemistry

(HP/C) Manager.

Based

on the report reviews

and discussions,

the following

conclusions

were drawn:

The licensee's

emphasis

concerning investigation of

radiological

events

had shifted toward evaluation of incidents

whether

or not the incidents

were initially deemed reportable.

This change is in accordance

with commitments

discussed

with

NRC regional

management

(see

Inspection

Report 50-397/88-08).

.However,

the wording-of

PPM 11.2. 19. 1 indicated that the

procedure

was intended only for non-reportable

events.

In practice, virtually all radiological events

were being

reported

on

RORs,

except

as

noted above.

Those incidents with

some question

as to reportability had dual documentation,

in

that

NCRs were also initiated.

No documented

incidents for the period reviewed .were observed

to have received

an inadequate

level of review by the licensee.

See paragraph

3, below, item 50-397/88-36-01,

for further discussion

of problem identification and correction.

Audits and

A

raisal

The following selected

Quality Assurance

(QA) Audits and Quality

Control

(QC) surveillances

were reviewed:

Audit

(2-87-371)

Title

PPM 11.2. 10.5 Area Radiation Monitor

Calibration

Date

11/12/87

(2-88-042)

(2-88-183)

(2-88-213)

(2-88-440)

Use of Radwaste

Drums and Control

2/10/88

Area Radiation Monitor Calibration/Setpoints

9/22/88

Radiological

Occurrence

Reports - Corrective

(Open)

Action/Followup

1"

Radiological

Environmental

Monitoring Program 5/18/88

(REMP)

Personnel

performing the audits

had the qualifications

and independence

required

by the licensee's

program.

Response

to audit findings, for

those audits

reviewed,

was

more timely and self-critical than-had

been

previously observed.

In particular,

gA audit 088-440 findings were

closed

on schedule

(see Inspection

Report 50-397/88-28).

Other aspects

of the licensee's

program in this area

were discussed

in

Inspection

Report 50-397/88-33.

The licensee's

program appeared

capable

of meeting its safety objectives.

No violations or deviations

were identified.

3.

~Fo1 1 owu

A.

Followu

on Items of t<oncom liance

and Deviations

50-397/88-22-04

Closed

This matter refens to the licensee's

corrective action related to unauthorized entry into high radiation

areas

and

an observed

lack of knowledge of access

controls

by plant

personnel.

The licensee

had produced

a videotape presentation

as

part of their corrective action.

The presentation

addressed,

but

did not stress,

the unacceptability

of disregarding

access

controls

for high radiation areas.

The access

controls

and other safety

aspects

of work in and around high radiation areas

were presented.

Based

on the licensee's

commitment to make the presentation

to all

personnel,

this matter is considered

closed

(50-397/88-22-04

closed).

B.

~Fol 1 owu

50-397/88-28-01

0 en

This refers to the licensee efforts to

improve continuous air monitor (CAN) availability.

Representative

maintenance

records

were reviewed.

The two primary means of failure

appeared

to be

a lack of reproducibility on weekly source

checks,

and repetitive or unrepaired

detector

fai lures.

In one case,

a

CAN

on the refueling floor of the Reactor

Building (RB), was recorded

as

having failed source

checks

from 8/1/88 to the time of the

inspection, without corrective maintenance

having been performed.

Another

CAM, in the

Radwaste

Building (RMB), had

a deficiency tag

which indicated it had

an inoperable detector.

Several

other

CAMs

'ere

recorded

as having failed source

checks

on a regular basis.

All appeared

to have retained their sampling capability.

The matter

was discussed

with the licensee,

who stated that the weekly source

checks

were being evaluated

as to applicability and usefulness.

This matter will remain

open (50-397/88-28-01

Open).

50-397/88-36-01

0 en

This refers to the licensee identified

potential

degradation

of post-accident

monitoring capability.

The

licensee

determined that during operation of the Standby

Gas

Treatment

(SGT) system for ventilation of the secondary

containment,

as allowed in an accident condition, continued operability of the

Main Plant Vent (MPV) stack effluent monitor (REA-SR-37) was not

assured

for the low/intermediate

ranges.

The post-accident

particulate/iodine

sampling unit is started

by an alarm condition on

the intermediate

range

MPV noble

gas channel.

The possible

inoperability

was caused

by the automatic

sample flow control

system,

which maintains sample/effluent

flow ratio and isokinetic

sampling

by following effluent flow.

As effluent flow rate is

reduced

from approximately 98,000

cfm to the maximum

SGT flow rate

of 4000 cfm, the control signal for sample flow shuts the valve.

See Inspection

Report 50-397/88-33 for discussion of non-accident

operability.

On October ll, 1988, the licensee

requested

a teleconference

to

discuss

the issue.

The participants

were:

For

NRC

Re ion V

Senior Resident

Inspector

Radiation Specialist

Chief,

Emergency

Preparedness

and Radiological

Protection

Branch

(EP8RPB)

Reactor Projects

Inspector

(WNP-2)

For the Licensee

Assistant Plant Manager

Assistant Plant Technical

Manager

Plant Engineering Supervisor

Health Physics/Chem'istry

(HP/C) Manager

Compliance

Engineer

The licensee

discussed

reporting requirements,

the possibility that

the system

was not indeed inoperable,

and their plans for resolution

by testing the system.

The licensee

stated that although they had concluded

the matter

was

not specifically reportable, their commitment to plant improvement

made it desirable

to keep

Region

V staff apprised of such matters.

The basis for non-reportability was the licensee's

conclusion that

compensatory

information was available,

as required

by Regulatory

Guide

(RG) 1.97,

Revision 3,

May 1983, Instrumentation for Li ht-

Water-Cooled Nuclear

Power Plants to Assess

Plant

and Environs

Conditions Durin

and Followin

an Accident.

The

EP8RPB Chief

expressed

concern, that should the monitor be determined to have

been

inoperable

since before the plant was licensed, it would result in

the conclusion that the licensee

had not met the plant description,

of having the

RG 1.97 systems

in place,

which would be reportable

as

required

by license condition 2. F.

The licensee

responded

to the concern with a proposal

to test the

system

immediately with a simulated

SGT - magnitude flow, and to

evaluate

by means of a test the actual

operating conditions

under

which ventilation system flows would allow operation of SGT in lieu

of normal

RB ventilation.

The licensee

conducted

the test

a short

time after the conclusion of the discussion.

The licensee

stated

that the test results indicated, that with an effluent flow signal

equivalent to

SGT flow, a sample flow rate of approximately

0. 18 cfm

was obtained.

With a sample line 60 feet in length and 1/2 inch

inner diameter,

the transit time would be approximately

30 seconds

for sampled air to reach the noble gas monitor.

The inspector

discussed

with the licensee

the uncertainty associated

with normal

effluent flow versus

SGT flow as

a motive force for the sample.

The

licensee

stated that at the next available

shutdown the system would

be tested

under actual

SGT flow conditions,

and the results

provided

to the inspector.

Although the sample test which was performed did

not quantify actual conditions,

and

no characterization

was

made

as

to sampling characteristics

for iodines

and particulates,

the

inspector

concluded that the noble

gas intermediate

range monitor

appeared

to be capable

of performing its safety function.

Pending

further testing,

committed to by the licensee,

this matter will

remain

open (50-397/88-36-01'pen).

No violations or deviations

were identified.

4.

Facilities

and

E ui ment

The licensee

had not made

any major equipment

changes

since the last

inspection of this area.

In reviewing

RORs (see

paragraph

2, above),

the

inspector

noted that the licensee

had increased

the storage facilities

for radioactive materials

outside the protected

area.

One

NCR,

02-88-044,

was related to workers not trained at WNP-2, apparently

knocking over and not restoring radiological postings for the storage

area in Warehouse

85 (Building 80).

The

ROR indicated that additional

material

was being stored in the warehouse,

outside the locked enclosure.

The enclosure

was originally constructed

to control access

to radioactive

sources,

used

by the licensee for calibration

and testing,

during

construction.

A review of the licensee's

Process

Control

Program,

discussions

with the licensee,

and tours of the storage

locations,

revealed

the following:

Licensee

Procedure

PPM 1. 1.3, Plant

Res onsibilities, Revision 10,

dated 03/23/88,

states

that the

HP/C Manager is responsible for,

"...plant receipt

and storage of radioactive materials...."

PPM 1. 11.3, Health

Ph sics

Pro ram, Revision 4, dated 04/04/88,

states

that the

HP/C Manager shall

be responsible

for:

".

~ . documentation of radioactive material receipts,

storage,

and

transfer."

PPM 11.2. 14.3, Stora

e of Radioactive Material, Revision 3, dated

06/30/87,

step 11.2. 14.3.4,

Precautions

and Limitations, states

in

par4:

"Non-licensed material or by-product materials

produced at

the facility are exempt from this procedure."

PPM 11.2. 14.9, Stora

e and Control of Site Generated

Radioactive Material,

was listed in the licensee's

table of contents

for the Health Physics series

of PPMs.

However,

no copy was

available,

and it was determined that the procedure title was

apparently installed in the licensee's

computerized tracking system

on November 12,

1985.

The licensee

was not able to provide

information regarding the original purpose for the procedure,

and

stated that the procedure

had not been written or reviewed

by the

Plant Operations

Committee

(POC).

PPM 11. 2. 23. 15,

Extended

Stor a

e of Radioactive Material, was,

as

stated

by the licensee,

in the process

of being written at the time

of the inspection.

The origination date

was 9/20/88.

The licensee

stated that the purpose

was to establish

an inventory control

method

for radioactive wastes

awaiting disposal.

The licensee further

stated that the procedure

did not specify storage

locations or

address

non-waste

contaminated

equipment.

PPM 1. 12. 1, Radioactive

Waste

Mana ement

Pro ram, Revision 3, dated

12/14/87,

under step

1. 12. 1.8.M, "Radioactive Waste Storage,

Handling,

and Shipping," states

in part:

"The on-site radioactive

waste storage

requirements

are outlined in

NRC Branch Technical,

Position

ETSB 11-3,

Rev.

2, July 1981."

ETSB 11-3, which is part of

section

11.4 of the Standard

Review Plan, states

in part:

"This

position paper sets forth minimum branch requirements...."

ETSB

11-3, Part III, "Waste Storage",

states

that storage of solidified

wastes

'should

be located indoors,

and that storage

areas for dry

wastes

and packaged

contaminated

equipment

should

be capable of

accommodating

one full offsite waste

shipment.

ETSB 11-3 does

not

address

non-waste

contaminated

equipment.

The licensee

had stored licensed

sources for WNP-2 in the locked

enclosure

in Warehouse

5.

The licensee

obtained permission

from NRC

to transfer WNP-l, 3,

and

5 licensed

sources

to WNP-2.

These

were

observed to be stored in the enclosure.

Contaminated

equipment

was

stored outside the locked enclosure

but within a posted

boundary.

All the equipment

appeared

to be appropriately labeled

and posted in

accordance

with 10 CFR 20 and/or

10 CFR 70,

as applicable.

The licensee

had stored additional

contaminated

equipment in what

appeared

to be weather-tight containers

(designated

"C-Yans" by the

licensee)

near the Plant Support Facility (PSF)

and near Warehouse

5.

Additionally, the licensee

had stored plastic-wrapped

components

and equipment for the Moisture Separator

Reheaters

(MSR) heat

exchanger

tube bundles,

which had been replaced

and were awaiting

disposal,

in a quonset

hut near the property line since March, 1987.

These

locations also appeared

to be properly posted,

although the

MSR parts were subject to some weather effects

due to the plastic

packaging

and numerous

holes in the quonset

hut structure,

the

concrete

pad of which was not bermed.

The licensee later provided

information to the effect that the maximum contamination level

on

the

MSR parts

was 16,000 disintegrations

per minute

(dpm) per 100

cm~.

The licensee

stated that the total activity for the

MSR

bundles

had been calculated,

but that

no specific calculation

was

available for the C-vans or other such equipment.

PPM 11.2.24. 1, Health

Ph sics

Work Routines,

Revision 4, dated

01/23/87, lists the Warehouse

5 storage

area

as

an area

included in

the weekly survey schedule,

and lists the warehouse

complex as

a

semi-annual

survey location.

The

MSR tube bundle storage

area

and

C-vans were not listed in

PPM 11.2.24. 1.

The

HP Supervisor stated

that surveys of those

areas

were performed approximately quarterly

under step 11.2.24. 1.5.G,

"Semi-Annual Routines,"

which lists site

building surveys

and states

in part:

"Any other areas

assigned

by

the Health Physics

Supervisor or designee."

Anal sis

Re ort (FSAR), part 2. 1. 1.3,

(page

2. 1-2,

amendment

36) states

in part:

"An area

encompassing

approximately

one square mile has

been

established

as the limit of the restricted

area.

~ .shown in Figure

2. 1-3..."

Review of Figure 2. 1-3 indicated that all the radioactive

material

storage

areas

identified by the inspector

were within the area

delineated

thereon.

The

FSAR did not appear to address

non-waste

radioactive material outside the plant itself, and stated generally in

Chapter ll that sufficient storage of dry active waste

was available

within the

RWB.

The licensee

was informed that the lack of documentation

of storage

areas

by the

HP/C manager,

the lack of a procedure for handling and storage of

non-waste

site-generated

radioactive material,

and the unincorporated

nature of routine surveys,

were considered

to be an unresolved

item.

The

issue of the definition of the restricted

area

was resolved sufficiently

to determine that radioactive material

was being stored in accordance

with 10 CFR 20. 203(e)

and (f).

This matter will remain

open pending

further review of the licensee's

procedures,

applicable

requirements,

and

quantification of the activity stored in the outside

areas

(50-397/88-36-02

unresolved).

An unresolved

item is one about which more information is required in

order to determine if it is an acceptable

item,

a deviation, or a

violation.

No violations or deviations

were identified.

Tours of the

RWB,

RB, and Turbine Building (TB) were conducted.

Independent

radiation surveys

were performed with an

NRC ion chamber

survey instrument

model

R0-2, Serial

0009154, calibrated 8-12-88 and

due

for calibration 11-12-88.

While touring the 467

elevation of the

RWB, the inspector

noted that the

gate for an area in the east valve gallery had

a hole in the anti-tamper

screening,

such that unauthorized individuals could reach through the

'ate

'to unlock it from the outside.

The licensee

had been maintaining

the area

locked due to fluctuation of dose rates in the

room of

approximately

1000 mr/hr.

At the time of the inspection,

no significant

change

appeared

to have occurred since the last inspection,

when dose

rates

were measured

at much less than

1000 mr/hr (see Inspection

Report

50-397/88-33,

paragraph

5).

When the inspector

informed the

HP

Supervisor,

the area

was immediately locked with a chain

and padlock and

the licensee

convened

a meeting to investigate

how the anti-tamper device

came to be inoperable.

The licensee

concluded

from discussion with

personnel

who had performed maintenance

on the lock that the original

installation

had been with a lock mechanism

on the right side of the

scissor

gate,

which had been

moved to the left side,

leaving the hole

through which the mechanism

had previously protruded.

The inspector

concurred with the licensee's

observation that the

HP escort for the lock

mechanism

work erred in not recognizing the reduction in security which

resulted.

The described

condition had existed

from the .time of

installation until the inspection.

The licensee

documented

the

investigation in accordance

with their problem-reporting

procedures.

Radioactive

resin liner movement in preparation for transport for

disposal

was observed.

It was noted that the licensee

did not have the

capability to attach/detach

handling equipment for the type of liner

being used.

Personnel

performing the liner movement stated that lifting

slings for

a liner reading

70 R/hr were removed

by having an individual

climb on top of the liner to remove the shackles

and slings.

The

licensee

was minimizing dose primarily by using experienced

workers in

order to minimize the time on top of the liner.

At approximately 1:00 p.m.

on October 10, 1988,

on the 422'levation of

the

RB, frisker model

L-177, serial

¹F091,

was found to have

no

indication on the instrument tag of the daily (24 hr) source

check

performed for the day,

as required

by

PPM 11.2.9.2,

Ludlum Model 177,

Revision 2, dated 4/20/87.

The inspector

informed the lead

HPT.

A few

minutes later,

an

HPT was observed to be using the frisker for a survey

of the "B" RHR pump room, in preparation for release

of the contaminated

area.

Discussion with the

HPT revealed that

he was

unaware that

no daily

source

check was indicated.

PPM 11.2.9.2 step 11.2.9.20.5.B. l.e states

in part:

"Ensure that the instrument'as

been source

checked for the day that it

i s to be used. "

The HPT,

and several

persons

who had per formed whole body frisks after

exiting the "B" RHR room contaminated

area,

had not ensured that the

source

check

had been performed.

The matter

was brought to the attention

of the

HP Supervisor,

who stated that the daily source

check checklist

indicated that the instrument

had been

checked,

and that the secondary

documentation

on the instrument tag was what had been missed.

The tag

was subsequently

completed properly.

At approximately 8:00 a.m.

on October 13,

1988, at the entry to the

counting

room on the 487'levation of the

RWB, frisker model

L177,

serial ¹F144, it was found that notation of the daily source

check was

missing

on the instrument tag, although it was indicated

on the daily

checklist.

Chemistry personnel

who had performed whole body frisks were

observed

to not check the tag.

When self-frisking was discussed

with the

chemistry personnel,

the view expressed

was that the source

checks

were

the. responsibility of the

HP Department.

The inspector

reminded the

>>/>>/

"Instrument shall

have

been

source

checked within the past

24 hours2.777778e-4 days <br />0.00667 hours <br />3.968254e-5 weeks <br />9.132e-6 months <br />..."

and that the source

check tag is the

means of verification for frisker

users.

The matter of personnel

not verifying instrument operability

prior to use

was discussed

with the

HP Supervisor,

who stated that

instrument verification would be stressed

to instrument

users

in the

plant.

At approximately 2:15

pm,

PDT,

on October 10,

1988, the radiation area

posting

and barricade for the Reactor

Core Isolation Cooling

Pump 81

(RCIC-P-1)

room was found to have

been

moved to one side

such that the

sign could not be read.

The sign and barricade for the other door to the

room was found to be in the

same condition.

Dose rates in the

room

measured

up to 10 mr/hr in accessible

areas,

and the licensee's

most

recent

survey identified the

room as

a radiation area.

10 CFR 20.202,

"Personnel

monitoring." states,

in part:

"(2) "Radiation area"

means

any area,

accessible

to personnel,

in which

there exists radiation, ... at such levels that

a major portion of the

body could receive in any one hour

a dose in excess

of 5 millirem,...."

10 CFR 20. 203, "Caution signs,

labels,

signals

and controls." states,

in

part:

"(b) Radiation areas.

Each radiation area shall

be conspicuously

posted

with a sign or signs bearing the radiation caution

symbol

and the words:"

"Caution "

1

"Radiation Area"

" Or "Danger""

1

The inspector

informed the

HP Supervisor,

who dispatched

an

HP foreman to

the

room.

While the inspector

and the foreman were discussing

the

matter,

and b'efore the postings

were restored,

an individual entered

the

room without replacing the sign on the side of the

room through which he

had entered.

The

HP foreman

asked the individual if he had been in

RCIC-P-1 room earlier.

He stated that he had, but that the sign had

already

been

down when

he

came in.

He further stated that

he had not

been through the other door.

The

HP foreman counseled

the individual on

posting restoration.

The inspector

discussed

the issue of radiological postings with the

HP

Supervisor

and the

HP/C Manager.

The matter

had been addressed

in a

number of previous inspections.

An apparent

reduction in such instances

had resulted in closing

an open item regarding the failure to restore

postings after entry (see Inspection

Report 50-397/88-33).

The inspector

expressed

concern that the above

was

a significant indication that the

problem was not yet resolved.

The failure to have the RCIC-P-1 room

posted

as

a radiation area is an apparent violation of 10 CFR 20.203

(50-397/88-36-03).

While touring the

RB on various elevations, it was observed that

equipment

was being left within the red/white tape boundaries

for several

safety-related

instrument racks.

The matter was later turned over to the

resident inspector for discussion with the licensee.

Near one area,

an

instrumentation

technician with whom the equipment

was discussed

stated

that it was not his, but that the red/white markers

were for very high

10

levels of radiation,

and that the inspector should discuss

the matter

with the

HP department.

Mhen the inspector

asked

about marking color,

t,ne sec.nnician,

after

some hesitation,

stated correctly that

yellow/magenta

were for radiation hazards,

and also correctly identified

the red/white markings with the red/white "Shift Supervisor's

approval

for entry" signs.

The technician stated

he had not yet viewed the video

tape presentation

discussed

in paragraph

3, above.

With regard to fire protection,

in room R415 of the

RB, by instrument

rack E-IR-H22/P027,

a rubber

hose

had been left coiled in the corner.

A

sign

on the door stated:

"Unattended

combustibles

not allowed in room

R415."

Door R512 on the 522'levation of the

RB, which was not

specif'ically posted

as

a fire door,

was found propped

open with a piece

of 2" pipe.

The pipe presented

an unrestrained tripping hazard

when the

door was

opened.

Both matters

were immediately corrected

when brought to

the attention of the licensee.

Housekeeping

had deteriorated slightly from the good conditions

noted

during the last inspection.

Several

areas

were noted to have small

amounts of used plastic

and protective clothing in corners

and at

step-off pads

from contaminated

areas.

Although some contaminated

areas

had

been

reduced

or eliminated

by the licensee,

the total area did not

appear

to have

changed significantly.

Although the matter of area postings

appeared

to be

a recurring problem,

the licensee's

program,

in general,

appeared

capable of meeting its

safety objectives.

Other than the item identified as 50-397/88-36-03,

no violations or

deviations

were identified.

6.

Exit Interview

The inspector

met with those individuals denoted in paragraph

1 at the

conclusion of the inspection

on October 14,

1988.

The scope

and findings

of the inspection

were summarized.

The licensee

acknowledged

the

apparent violation discussed

in paragraph

5, above.

The licensee

provided additional information regarding the unresolved

item discussed

in paragraph

4, above,

and committed to providing the inspector with an

approximate quantification of the radioactive material contained in the

storage

areas

noted therein.

'