ML20003H854
| ML20003H854 | |
| Person / Time | |
|---|---|
| Site: | 07100437 |
| Issue date: | 04/17/1981 |
| From: | Slemp G ADVEX CORP. |
| To: | |
| Shared Package | |
| ML20003H853 | List: |
| References | |
| 19025, NUDOCS 8105080057 | |
| Download: ML20003H854 (4) | |
Text
Teleshne (804) 82M9M
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CORPORATION 1.1 FLOYD THOMPSON OR.
- P.O. BOX T263 HAMPTON VIRCINA 236%
10 CFR PART 71 QUrTITY ASSURANCE PROGR.Of For Industrial
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j Radiography Licenses i
l Approved:
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l G.E.SLEMP,byAGER Quality Assurance Date: April 17, 1981 l
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f 8105080051 19025 PREC5?ON \\tACHIAING & FABRICATION AIRFLOW RESEARCH S?ECIALTIES MECHANICAL PROTOTYPE EQUIPMENT NONDESTRt CTIVE EXAMINATION
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CRGANIZATION CHART FOR ADVEX CORPORATIO:I INDUSTRIAL RADICCRAPHIC OPERATIONS President R, L. Coble h
2 Quality Assurance Ma.itger
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- C.
E. Slemp l
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I NDE Supervisor (Administrative - Position not I
filled at this time) 3 I
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I Radiographers Radiographers Assistants
- Radiation Safety Officer i
Radiation Safety Responsibility
~ = 7.
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1 2.
QUALITY ASSURANCE PROGRAM The Management of ADVEX CORPORATION establishes and implements this QA Program.
Training, prior to engagement, for all QA functions is required according to written procedures. Procedures, as referred to herein, includes Advex's Operating and Emergency Procedures
' governing the Safe Use of Radioactive Isotopes (as approved by the U. S. NRC) and/or written procedures approved by Advex Management.
Q. A. Proigram revisions will be made according to written procedures.
The QA Program will ensure that all defined QC procedures, Engineering procedures, and specific provisions of the package design approval are satisfied. Tha QA Program will-emphasize control of the characteristics of the package which are critical to safety.
i The Radiation Safety Officer shall assure that all' radioactive i
material shipping packages are designed and manufactured under a QA Program approved by the Nuclear Regulatory Commission for all packages designed or fabricated af ter January 1,1979. This requirement will be satisified by receiving a certifications to this effect from the manufacturer.
3.
DOCUMENT CONTROL All Documents related to a specific shipping package will be controlled through the use of written procedures. All document l
changes will be performed according to written procedures.
The Radiation Safety Officer shall ensuret that all QA functions are conducted in accordance with the latest applicable changes to these documents.
4.
HANDLING, STORAGE, AND SHIPPING Written safety proceudres concerning the handling, storage, and shipping of pacakages for certain special form radioactive material will be followed. Shipments will not be made unless all tests certi-fications, acceptances, and final inspections have been completed.
Work instructions will be provided for handling, storage, and shipping operations.
Radiography personnel shall perform the critical handling, storage, and shipping operations.
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INSPECTION, TEST,A.}DOPERATINGSTATUS Inspection, test, and operating status of packages for certain special form radicactive material will be indicated and controlled by written procedures. Status will te indicated by tag, label, marking, or log entry.
Jtatus of nonconfor=ing parts or packages will be positively maintained by written procedures.
Radiography personnel shall perform the required regulatory
' inspections and tests in accordance with written procedures. The Radiation Safety Officer shall ensure that these functions are performed.
6.
QUALITY ASSUR.CCE RECORDS
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Records of package approvals (including references / drawings and/or certifications), procurement, inspections, tests, operating logs, audit results, pdrsonnel training and qualifications and recorda of shipments will be maintained. Descriptions of equip =ent and written procedures will also be maintained.
These records will be maintained in accordance with written procedures. The records will be identified and retrievable. A list of these records, with their storage locations, will be main-tained by the Radiation Safety Officer.
7.
AUDITS Established schedules of audits of the QA Program will be per-formed using written check lists. Results of audits will be maintained j
and reported to management. Audit reports will be evaluated and l
deficient areas corrected. The audits will be dependent on the safety l
significance of the activity being audited, but each activity will be audited at least once per year. Audit reports will be maintained as part of the Quality Assurance records. Members of the audit team shall have no responsibility in the activity being audiced.
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