FDA Inspection
The Peavey Corporation dba Lynn Peavey Co.The Peavey Corporation dba Lynn Peavey Co. – FDA Inspection, Jan 10, 2023
Record Details
This FDA Inspection record concerns The Peavey Corporation dba Lynn Peavey Co., with an inspection on January 10, 2023, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 4d937b93-fc9a-43e0-a8e0-da2b784f4143
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1195222
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
FDA Citations
5- 21 CFR 820.20(c)Management review - Lack of or inadequate procedures
- 21 CFR 820.22Quality audits - Lack of or inadequate procedures
- 21 CFR 820.25(b)Training records
- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
- 21 CFR 820.75(a)Lack of or inadequate process validation
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Other FDA inspections of The Peavey Corporation dba Lynn Peavey Co.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| November 26, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 17, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 21, 2010 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for The Peavey Corporation dba Lynn Peavey Co.
- FDA Inspection 856700 - 2013-11-26
- FDA Inspection 747394 - 2011-06-17
- FDA Inspection 682226 - 2010-09-21
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