FDA Inspection
PeakVision IncPeakVision Inc – FDA Inspection, Mar 29, 2011
Record Details
This FDA Inspection record concerns PeakVision Inc, with an inspection on March 29, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- PeakVision Inc
- Inspection Date
- March 29, 2011
- Product Type
- Devices
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ID · b41ac775-e97d-4c54-ba37-c2b9d6c7e605
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 716464
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
2- 21 CFR 820.20(e)Quality System Procedures
- 21 CFR 803.17Lack of Written MDR Procedures
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