ML19276F396

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In Order to Approve QA Program,Requests Statements That quality-related Activities Will Be Performed W/Specified Equipment & Under Suitable Environ Conditions.Requests Statement That Records Are Identifiable & Retrievable
ML19276F396
Person / Time
Site: 07100090
Issue date: 03/13/1979
From: Macdonald C
NRC OFFICE OF NUCLEAR MATERIAL SAFETY & SAFEGUARDS (NMSS)
To: Lichtenberger H
ABB COMBUSTION ENGINEERING NUCLEAR FUEL (FORMERLY
References
NUDOCS 7903300057
Download: ML19276F396 (2)


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UNITED STATES

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NUCLEAR REGULATORY COMMISSION 3 %.

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WASHINGTON, D. C. 20555 bE['.<.>.

8 MAR 131979 FCTR: RHO 71-0090 Combustion Engineering, Inc.

ATTN: Mr. H. V. Lichtenberger 1000 Prospect Hill Road Windsor, CT 06095 Gentlemen:

This refers to your application dated June 23, 1978 requesting approval of your Quality Assurance (QA) program as meeting the QA program requirements of 10 CFR 571.51.

In connection with our review, we need the information identified in the enclosure to this letter.

Please submit seven copies of your response to the enclosed request for additional information within 30 days following receipt of this letter.

If you have any questions regarding this request, please feel free to contact Mr. Jim Conway at (301) 492-7741.

Sincerely, ar es

. MacDonald, Chief Transportation Branch Division of Fuel Cycle and Material Safety, NMSS

Enclosure:

Request for Additional Information 7903300 057

4 COMBUSTION Ef1GIf1EERING (71-0090)

REQUEST FOR ADDITIONAL INFORMATION 1.

Provide a statement that quality-related activities are performed with specified equipment and under suitable environmental conditions, and prerequisites have been satisfied prior to inspection and test.

2.

Provide a statement that bypassing of required inspections, tests, and other critical operations is proceduraily controlled.

3.

Provide a statement that records are identifiable and retrievable.

4.

Provide a statement that inspection and test records contain the following where applicable:

a.

A description of the type of observation.

b.

The date and results of the inspection or test.

c.

Information related to conditions adverse to quality.

d.

Inspector or data recorder identification.

e.

Evidence as to the acceptatility of the.esults.

5.

Provide a statement that audit reports will be evaluated and deficient areas corrected.