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| number = ML18005A357
| number = ML18005A357
| issue date = 10/24/1986
| issue date = 10/24/1986
| title = Rev 1 to Administrative Procedure AP-026, Corrective Action Program.
| title = Rev 1 to Administrative Procedure AP-026, Corrective Action Program
| author name = Willis J
| author name = Willis J
| author affiliation = CAROLINA POWER & LIGHT CO.
| author affiliation = CAROLINA POWER & LIGHT CO.
Line 17: Line 17:


=Text=
=Text=
{{#Wiki_filter:.CAROLINA POWER 6 LIGHT COMPANY SHEARON HARRIS NUCLEAR POWER PLANT PLANT OPERATING MANUAL VOLUME 1 PART 1 PROCEDURE TYPE:     ADMINISTRATIVE PROCEDURE (AP)
{{#Wiki_filter:.CAROLINA POWER 6 LIGHT COMPANY SHEARON HARRIS NUCLEAR POWER PLANT PLANT OPERATING MANUAL VOLUME 1
NUMBER:             AP-026 TITLE:               CORRECTIVE ACTION PROGRAM V OS   gg APPROVED:                                          fez+ R ignacure                  Dace 8803ih0343 880222 PDR   ADOCK 05000400                           Page 1 of 8 G                  PDR
PART 1
PROCEDURE TYPE:
ADMINISTRATIVE PROCEDURE (AP)
NUMBER:
AP-026 TITLE:
CORRECTIVE ACTION PROGRAM APPROVED:
ignacure V
OS gg fez+ R Dace 8803ih0343 880222 PDR ADOCK 05000400 G
PDR Page 1 of 8


OS1 l                               LIST OF EFFECTIVE PAGES 0
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OS1 0    1 2.0 0
OS1 0
TOPIC PURPOSE TABLE OF CONTENTS PAGE 4
TOPIC TABLE OF CONTENTS PAGE 1 0 PURPOSE
REFERENCES 3.0                                           4 RESPONSIBILITIES 4.0                                            4 DEFINITIONS/ABBREVIATIONS 5.0                                            5 PROCEDURES 6 0                                            5 DIAGRAMS/ATTACHMENTS 6
t P4 A
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    *
      ~ AP-026 Rev. 1 Page 3 of 8


OS1 1.0   PURPOSE This procedure establishes administrative requirements in support of the SHNPP Corrective Action Program (CAP) ~ This procedure describes a comprehensive tracking program which will be utilized to assure identified action items are completed in a timel.y manner and establishes the requirement that a status summary is reported on a routine basis.
==2.0 REFERENCES==
3.0 RESPONSIBILITIES 4.0 DEFINITIONS/ABBREVIATIONS 5.0 PROCEDURES 6 0 DIAGRAMS/ATTACHMENTS 4
4 4
5 5
6 t
P4 A
- ~
AP-026 Rev.
1 Page 3 of 8
~
* OS1 1.0 PURPOSE This procedure establishes administrative requirements in support of the SHNPP Corrective Action Program (CAP) ~
This procedure describes a comprehensive tracking program which will be utilized to assure identified action items are completed in a timel.y manner and establishes the requirement that a status summary is reported on a routine basis.


==2.0   REFERENCES==
==2.0 REFERENCES==
2.1 Nuclear Operations Department Procedure 7.24, Corrective Action Program.
2.2 Operating Experience Feedback (ONSI-1)'.
2.3 Procedure for Corporate.QA Audits, CQAD 80-1.
3' RESPONSIBILITIES 3.1 Director - Regulatory Compliance is responsible for maintaining the CAP ~
3.2 Unit Managers and supervisors will assure accurate and appropriate information is forwarded to the Director-Regulatory Compliance for input into the CAP Action Item List and the CAP Report.
3.3 Regulatory Compliance Unit shall:
a.
Evaluate items identified by other groups for inclusion in the CAP program.
b.
Review all incoming and outgoing correspondence under Regulatory Compliance responsibility for items appropriate to be entered into the CAP tracking system.
c.
Monitor NRC, ANI and INPO inspection activities and enter plant commitments and corrective action into the CAP.
d.
Identify and enter into the CAP other action items requiring tracking and timely close out, including NRC reporting requirements such as LERs, Technical Specification routine reports.
e.
Tracking Quality Assurance NCRs issued to Harris Plant Operations Section organizations using the CAP in order to assure timely close out.
f.
Maintain the CAP current.
AP-026 Rev.
1 Page 4 of 8 I ~


2.1  Nuclear Operations Department Procedure 7.24, Corrective Action Program.
Osl 3.0 RESPONSIBILITIES (Cont'd) 3.4 Organizations AfEected - any CPSL personnel may be affected by the requirements oE this procedure.
2.2  Operating Experience Feedback (ONSI-1)'.
4.0 DEFINITIONS/ABBREUIATIONS Mone Applicable 5 '
2.3  Procedure    for  Corporate.QA Audits,  CQAD 80-1.
PROCEDURE 5.1 CAP Action Item List 1.
3 '  RESPONSIBILITIES 3.1  Director  -  Regulatory Compliance is responsible for maintaining the CAP ~
The CAP Action Items List will'be used to evaluate and track problem areas requiring corrective action such as:
3.2  Unit Managers and supervisors will assure accurate and appropriate information is forwarded to the Director-Regulatory Compliance for input into the CAP Action Item List and the CAP Report.
a.
3.3  Regulatory Compliance Unit shall:
Action items assigned by Plant Management (e.g,,
: a. Evaluate items identified by other groups for inclusion in the CAP program.
: b. Review    all incoming and outgoing correspondence under Regulatory Compliance responsibility for items appropriate to be entered into the CAP tracking system.
: c. Monitor NRC, ANI and INPO inspection activities and enter plant commitments and corrective action into the CAP.
: d. Identify and enter into the CAP other action items requiring tracking and timely close out, including    NRC reporting requirements such as LERs, Technical Specification routine reports.
: e. Tracking Quality Assurance NCRs issued to Harris Plant Operations Section organizations using the CAP in order to assure timely close out.
: f. Maintain the    CAP  current.
AP-026 Rev. 1                                              Page 4 of 8 I~
          '
 
Osl 3.0 RESPONSIBILITIES       (Cont'd) 3.4 Organizations AfEected - any CPSL personnel         may be   affected by the requirements oE this procedure.
4.0 DEFINITIONS/ABBREUIATIONS Mone   Applicable 5 ' PROCEDURE 5.1 CAP Action Item List
: 1. The CAP   Action Items List   will'be used to evaluate and track problem areas requiring corrective action         such as:
: a. Action items assigned by Plant Management (e.g,,
internal. actions required to cl.ear CAP Items).
internal. actions required to cl.ear CAP Items).
: b. Commitments   to non-CPSL organizations (e.g.,     NRC, INPO) ~
b.
: c. Commitments   to other CP&L organizations (e.g.,
Commitments to non-CPSL organizations (e.g.,
: NRC, INPO) ~
c.
Commitments to other CP&L organizations (e.g.,
Corporate QuaLity Assurance (CQA), Corporate Nuclear Safety (CNS)).
Corporate QuaLity Assurance (CQA), Corporate Nuclear Safety (CNS)).
: d. PNSC Action Items.
d.
: e. Response   to external audits.
PNSC Action Items.
E. Other items as appropriate.
e.
Items   vill   be entered and deleted from the     CAP Action Item List as Eollovs:
 
: 2. The Regulatory Compliance Unit       vill enter items into the CAP Action Item List and track those items until they are documented as resolved.
===Response===
: 3. The   Director   - Regulatory CompLiance, or his designee, will assign responsibility for       the resolution of CAP items by using the top portion oE Attachment 1, CAP
to external audits.
          . Action Assignment Form.
E.
: 4. To   request removaL/closeout of an item from the CAP program, the responsible supervisor or manager shall return Attachment 1 to the Director - Regulatory Compliance vith the bottom section completed and signed. Specific reference shall   be made to indicate how the item vas addressed,       or documentation verifying completion of'the assigned item (i.e., a copy of a revised procedure page or other documents) or the equivalent information on another signed document may be provided.
Other items as appropriate.
AP-026 Rev. 1                                                   Page 5 of 8
Items vill be entered and deleted from the CAP Action Item List as Eollovs:
2.
The Regulatory Compliance Unit vill enter items into the CAP Action Item List and track those items until they are documented as resolved.
3.
The Director - Regulatory CompLiance, or his designee, will assign responsibility for the resolution of CAP items by using the top portion oE Attachment 1,
CAP
. Action Assignment Form.
4.
To request removaL/closeout of an item from the CAP
: program, the responsible supervisor or manager shall return Attachment 1 to the Director - Regulatory Compliance vith the bottom section completed and signed.
Specific reference shall be made to indicate how the item vas addressed, or documentation verifying completion of'the assigned item (i.e.,
a copy of a revised procedure page or other documents) or the equivalent information on another signed document may be provided.
AP-026 Rev.
1 Page 5 of 8


OSL 5 '   PROCEDURES     (Cont'd) 5 ~ The CAP       Action Item List Printout of Items should be distributed to plant management by the first working day of each week.
OSL 5 '
: 6. To t'ransfer     'responsibility of a CAP Action Item from the assigned organization to another organization requi res acknowledgement by both organizations managers that said action is taking pLace.
PROCEDURES (Cont'd) 5 ~
  ~
The CAP Action Item List Printout of Items should be distributed to plant management by the first working day of each week.
l I      7 ~  Priority of        CAP  Item:
6.
      'I a
To t'ransfer 'responsibility of a CAP Action Item from the assigned organization to another organization requi res acknowledgement by both organizations managers that said action is taking pLace.
      -I               a. The      onsite originator of the CAP item will set the t
I
priority. The following criteria is a guideline a
~ l
  -= ~
'I
        ~                    which may be used for establishing the CAP
-I a
        <<
t a ~
priority.
-=~
I I  ~
        'I PRIORITY-1:
Highest      priority work  items represting a perceived imminent hazard to nuclear safety, personnel or unit generation.
I
I
    <<I                       PRIORITY-2:
'I I ~
7 ~
Priority of CAP Item:
a.
PRIORITY-1:
The onsite originator of the CAP item will set the priority.
The following criteria is a guideline which may be used for establishing the CAP priority.
Highest priority work items represting a perceived imminent hazard to nuclear safety, personnel or unit generation.
I
<<I PRIORITY-2:
Required work items representing commitments to regulatory agencies and management.
Required work items representing commitments to regulatory agencies and management.
PRIORITY-3:
PRIORITY-3:
Line 99: Line 146:
Routing work items having a moderate effect on nuclear safety, personnel safety, unit operation, or a moderate cost benefit.
Routing work items having a moderate effect on nuclear safety, personnel safety, unit operation, or a moderate cost benefit.
PRIORITY-5:
PRIORITY-5:
Routine work items having a nomi'naL     effect     on nuclear safety, personnel. safety, unit operations p                          or a normal. cost benefit.
p I<<l b.
I<<l
Routine work items having a nomi'naL effect on nuclear safety, personnel.
: b.      Priority     1 and 2 items have firm dates controlled by management     and the due date will not be changed
safety, unit operations or a normal. cost benefit.
                                . ithout the   agreement of the Plant General Manager.
Priority 1 and 2 items have firm dates controlled by management and the due date will not be changed
AP-026 Rev. l                                                     Page 6   of   8
. ithout the agreement of the Plant General Manager.
                                                                <<            ~ "<<s, <<  - = <<<<
AP-026 Rev. l Page 6 of 8 s
s                                    I
~ "<<s,
=
I


Osl 5.1   CAP Action Item List (Cont'd)
Osl 5.1 CAP Action Item List (Cont'd) c.
: c.   . Priority 3, 4, and 5 items have Elexibility in their due dates and can be changed based on the items priority content and availability of resources. A speed memo to Reg. Compliance with new compLetion date will extend the original. due date. This does not include QA/QC items which must go through the proper QA/QC ChanneLs Eor
. Priority 3, 4, and 5 items have Elexibility in their due dates and can be changed based on the items priority content and availability of resources.
                ~
A speed memo to Reg.
Compliance with new compLetion date will extend the original. due date.
This does not include QA/QC items which must go through the proper QA/QC ChanneLs Eor
~
extensions.
extensions.
5.2   uarterl   CAP Summer Re ort The Regulatory CompLiance Unit will prepare a CAP Summary Quarterly Report covering the operation of the program Eor the.
5.2 uarterl CAP Summer Re ort The Regulatory CompLiance Unit will prepare a
previous quarter. The report for the previous quarter will be forwarded to the Vice President - Harris Nuclear Project within thirty (30) days from the end of the previous quarter.
CAP Summary Quarterly Report covering the operation of the program Eor the.
6.0   DIAGRAMS/ATTACHMENTS Cap Action Assignment Form
previous quarter.
The report for the previous quarter will be forwarded to the Vice President - Harris Nuclear Project within thirty (30) days from the end of the previous quarter.
6.0 DIAGRAMS/ATTACHMENTS Cap Action Assignment Form
~ ~
~ ~
  'I AP-026 Rev. 1                                             Page 7 of 8
'I AP-026 Rev.
1 Page 7 of 8


Osl Attachment 1 CAP       Action Assignment   Form Date:
Osl Attachment 1
CAP Action Assignment Form Date:
Priority:
Priority:
TO:
TO:
FROM:   Director   - Regulatory Compliance The Following   CAP Action Item Is Assigned For            ur Disposition:
FROM:
CAP  item No.:                                                   ate  .
Director - Regulatory Compliance The Following CAP item No.:


==
==
Description:==
Description:==
 
CAP Action Item Is Assigned For ur Disposition:
Source Document W ~ '~
ate Source Document FROM:
                                    ~ I FROM:
W
                                    'I TO:   Directort',v R   I;atoryl 'Compliance
~ '~
                                'hl
~
                              ~   1 The +oya     CAP     Action Item Has Been Completed.
I
'I TO:
Directort',v R
I;atory 'Compliance l
'hl
~
1 The +oya CAP Action Item Has Been Completed.
Resolution.'Attach Supporting Documentation):
Resolution.'Attach Supporting Documentation):
Signature'.                                             Date:
Signature'.
(Form AP-026-1.-1)
Date:
Ae. i/>
Ae. i/>
(Form AP-026-1.-1)                                                                ! Au S'-C.b'7 AP"026 Rev. 1                                                       Page 8 of 8}}
Au S'-C.b'7 AP"026 Rev.
1 Page 8 of 8}}

Latest revision as of 07:12, 7 January 2025

Rev 1 to Administrative Procedure AP-026, Corrective Action Program
ML18005A357
Person / Time
Site: Harris 
Issue date: 10/24/1986
From: Joseph Willis
CAROLINA POWER & LIGHT CO.
To:
Shared Package
ML18005A336 List:
References
AP-026, AP-26, NUDOCS 8803160343
Download: ML18005A357 (8)


Text

.CAROLINA POWER 6 LIGHT COMPANY SHEARON HARRIS NUCLEAR POWER PLANT PLANT OPERATING MANUAL VOLUME 1

PART 1

PROCEDURE TYPE:

ADMINISTRATIVE PROCEDURE (AP)

NUMBER:

AP-026 TITLE:

CORRECTIVE ACTION PROGRAM APPROVED:

ignacure V

OS gg fez+ R Dace 8803ih0343 880222 PDR ADOCK 05000400 G

PDR Page 1 of 8

OS1 l~0

~Pa e

1 thru 8

LEP, 5
LEP, 8

LIST OF EFFECTIVE PAGES Revision AC-1/1 AC"1/2 l

4 5

0 AP-026 Rev.

1 Page 2 of 8 l

'hl s ~

l

~I

~'

P s

. ~

OS1 0

TOPIC TABLE OF CONTENTS PAGE 1 0 PURPOSE

2.0 REFERENCES

3.0 RESPONSIBILITIES 4.0 DEFINITIONS/ABBREVIATIONS 5.0 PROCEDURES 6 0 DIAGRAMS/ATTACHMENTS 4

4 4

5 5

6 t

P4 A

- ~

AP-026 Rev.

1 Page 3 of 8

~

  • OS1 1.0 PURPOSE This procedure establishes administrative requirements in support of the SHNPP Corrective Action Program (CAP) ~

This procedure describes a comprehensive tracking program which will be utilized to assure identified action items are completed in a timel.y manner and establishes the requirement that a status summary is reported on a routine basis.

2.0 REFERENCES

2.1 Nuclear Operations Department Procedure 7.24, Corrective Action Program.

2.2 Operating Experience Feedback (ONSI-1)'.

2.3 Procedure for Corporate.QA Audits, CQAD 80-1.

3' RESPONSIBILITIES 3.1 Director - Regulatory Compliance is responsible for maintaining the CAP ~

3.2 Unit Managers and supervisors will assure accurate and appropriate information is forwarded to the Director-Regulatory Compliance for input into the CAP Action Item List and the CAP Report.

3.3 Regulatory Compliance Unit shall:

a.

Evaluate items identified by other groups for inclusion in the CAP program.

b.

Review all incoming and outgoing correspondence under Regulatory Compliance responsibility for items appropriate to be entered into the CAP tracking system.

c.

Monitor NRC, ANI and INPO inspection activities and enter plant commitments and corrective action into the CAP.

d.

Identify and enter into the CAP other action items requiring tracking and timely close out, including NRC reporting requirements such as LERs, Technical Specification routine reports.

e.

Tracking Quality Assurance NCRs issued to Harris Plant Operations Section organizations using the CAP in order to assure timely close out.

f.

Maintain the CAP current.

AP-026 Rev.

1 Page 4 of 8 I ~

Osl 3.0 RESPONSIBILITIES (Cont'd) 3.4 Organizations AfEected - any CPSL personnel may be affected by the requirements oE this procedure.

4.0 DEFINITIONS/ABBREUIATIONS Mone Applicable 5 '

PROCEDURE 5.1 CAP Action Item List 1.

The CAP Action Items List will'be used to evaluate and track problem areas requiring corrective action such as:

a.

Action items assigned by Plant Management (e.g,,

internal. actions required to cl.ear CAP Items).

b.

Commitments to non-CPSL organizations (e.g.,

NRC, INPO) ~

c.

Commitments to other CP&L organizations (e.g.,

Corporate QuaLity Assurance (CQA), Corporate Nuclear Safety (CNS)).

d.

PNSC Action Items.

e.

Response

to external audits.

E.

Other items as appropriate.

Items vill be entered and deleted from the CAP Action Item List as Eollovs:

2.

The Regulatory Compliance Unit vill enter items into the CAP Action Item List and track those items until they are documented as resolved.

3.

The Director - Regulatory CompLiance, or his designee, will assign responsibility for the resolution of CAP items by using the top portion oE Attachment 1,

CAP

. Action Assignment Form.

4.

To request removaL/closeout of an item from the CAP

program, the responsible supervisor or manager shall return Attachment 1 to the Director - Regulatory Compliance vith the bottom section completed and signed.

Specific reference shall be made to indicate how the item vas addressed, or documentation verifying completion of'the assigned item (i.e.,

a copy of a revised procedure page or other documents) or the equivalent information on another signed document may be provided.

AP-026 Rev.

1 Page 5 of 8

OSL 5 '

PROCEDURES (Cont'd) 5 ~

The CAP Action Item List Printout of Items should be distributed to plant management by the first working day of each week.

6.

To t'ransfer 'responsibility of a CAP Action Item from the assigned organization to another organization requi res acknowledgement by both organizations managers that said action is taking pLace.

I

~ l

'I

-I a

t a ~

-=~

I

'I I ~

7 ~

Priority of CAP Item:

a.

PRIORITY-1:

The onsite originator of the CAP item will set the priority.

The following criteria is a guideline which may be used for establishing the CAP priority.

Highest priority work items represting a perceived imminent hazard to nuclear safety, personnel or unit generation.

I

<<I PRIORITY-2:

Required work items representing commitments to regulatory agencies and management.

PRIORITY-3:

Priority work items representing a significant potential hazard to nuclear safety, personnel safety, unit operation, or a significant cost benefit.

PRIORITY-4:

Routing work items having a moderate effect on nuclear safety, personnel safety, unit operation, or a moderate cost benefit.

PRIORITY-5:

p I<<l b.

Routine work items having a nomi'naL effect on nuclear safety, personnel.

safety, unit operations or a normal. cost benefit.

Priority 1 and 2 items have firm dates controlled by management and the due date will not be changed

. ithout the agreement of the Plant General Manager.

AP-026 Rev. l Page 6 of 8 s

~ "<<s,

=

I

Osl 5.1 CAP Action Item List (Cont'd) c.

. Priority 3, 4, and 5 items have Elexibility in their due dates and can be changed based on the items priority content and availability of resources.

A speed memo to Reg.

Compliance with new compLetion date will extend the original. due date.

This does not include QA/QC items which must go through the proper QA/QC ChanneLs Eor

~

extensions.

5.2 uarterl CAP Summer Re ort The Regulatory CompLiance Unit will prepare a

CAP Summary Quarterly Report covering the operation of the program Eor the.

previous quarter.

The report for the previous quarter will be forwarded to the Vice President - Harris Nuclear Project within thirty (30) days from the end of the previous quarter.

6.0 DIAGRAMS/ATTACHMENTS Cap Action Assignment Form

~ ~

'I AP-026 Rev.

1 Page 7 of 8

Osl Attachment 1

CAP Action Assignment Form Date:

Priority:

TO:

FROM:

Director - Regulatory Compliance The Following CAP item No.:

==

Description:==

CAP Action Item Is Assigned For ur Disposition:

ate Source Document FROM:

W

~ '~

~

I

'I TO:

Directort',v R

I;atory 'Compliance l

'hl

~

1 The +oya CAP Action Item Has Been Completed.

Resolution.'Attach Supporting Documentation):

Signature'.

(Form AP-026-1.-1)

Date:

Ae. i/>

Au S'-C.b'7 AP"026 Rev.

1 Page 8 of 8