FDA Inspection
Weinmann GmbhWeinmann Gmbh – FDA Inspection, Oct 21, 2010
Record Details
This FDA Inspection record concerns Weinmann Gmbh, with an inspection on October 21, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Weinmann Gmbh
- Inspection Date
- October 21, 2010
- Product Type
- Devices
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ID · b744f097-2293-41b1-9c57-462ca8cb949d
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 698574
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.70(i)Documentation of software validation
- 21 CFR 820.75(c)Documentation - review in response to changes or deviations
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Other FDA inspections of Weinmann Gmbh
1| Date | Classification | Office | Project area |
|---|---|---|---|
| June 25, 2015 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
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