ML19246C479
| ML19246C479 | |
| Person / Time | |
|---|---|
| Site: | 07100136 |
| Issue date: | 07/05/1979 |
| From: | Macdonald C NRC OFFICE OF NUCLEAR MATERIAL SAFETY & SAFEGUARDS (NMSS) |
| To: | Dandaneau L PARKER INDUSTRIAL X-RAY LABORATORY CORP. |
| References | |
| NUDOCS 7907250359 | |
| Download: ML19246C479 (2) | |
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UNITED STATES
! 'f 3,,,gh NUCLEAR REGULATORY COMMISSION g,_
,_ g WASHINGTON, D. C. 20555 o,.
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JUL 0 ~ 1979 t,
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FCTR: RHO 71-0136 Parker Industrial X-Ray Laboratory Corporation ATTN: Mr. L. F. Dandaneau 290 Governor Street East Hartford, CT 06108 Gentlemen:
This refers to your application dated June 30, 1978 requesting approval of your Quality Assurance (CA) 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 tc 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 contact Mr. Jack Spraul at (301) 492-7741.
Si ncerely, Charles E. MacDonald, Chief Transportation Branch Division of Fuel Cycle and Material Safety, NMSS
Enclosure:
Request for Additional Information 1;
401 225 7 907250 Hp
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THE PARKER INDUSTRIAL X-RAY LABORATORY CORPORATION (71-0136)
Recuest for Additional Information i
1.
In part III. identifj who (by tit.le) is responsible to insure that all QA functions a-coni:cted in accordance with the latest applicable documents.
2.
In part'I, ju st.. cement that radiography personr..i shall 'arform the regula'.oi.
sa.'rra inspections and tasts in accordance witn written procedu^es ana uic: rna r,adiation Safety Officer shall ensure that these function; a"e, erforned.
3.
In part VI, pr aide a rtatement that QA records will be maintained in accordance wita written procedures, that they will be identified and retrievable, and that a list of these records, with their storage location, will be maintained.
4.
In part VII, provide statements that the audits will be dependent on the safety significance of the activity being audited, but each activity will be audited at least once per year, that audit reports will be maintained as part of the quality asturance records, and that members of the audit team shall have no responsibility in the activity being audited.
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