FDA Inspection
OVESCO ENDOSCOPY AGOVESCO ENDOSCOPY AG – FDA Inspection, Aug 29, 2013
Record Details
This FDA Inspection record concerns OVESCO ENDOSCOPY AG, with an inspection on August 29, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- OVESCO ENDOSCOPY AG
- Inspection Date
- August 29, 2013
- Product Type
- Devices
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ID · 5cc5a217-4055-4012-a782-196f7510c8cc
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 851831
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
3- 21 CFR 820.20(c)Management review - defined interval, sufficient frequency
- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.22Quality audits - Lack of or inadequate procedures
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Other FDA inspections of OVESCO ENDOSCOPY AG
1| Date | Classification | Office | Project area |
|---|---|---|---|
| July 13, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for OVESCO ENDOSCOPY AG
- FDA Inspection 1052715 - 2017-07-13
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