FDA Inspection
DePuy BridgewaterDePuy Bridgewater – FDA Inspection, Oct 2, 2012
Record Details
This FDA Inspection record concerns DePuy Bridgewater, with an inspection on October 2, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- DePuy Bridgewater
- Inspection Date
- October 2, 2012
- Product Type
- Devices
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ID · bed28730-bf4a-4fcf-9ebf-702f26060ca2
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 801053
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.80(a)Lack of or inadequate procedures - Acceptance activities
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Other FDA inspections of DePuy Bridgewater
5| Date | Classification | Office | Project area |
|---|---|---|---|
| June 13, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 8, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 19, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 8, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 8, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for DePuy Bridgewater
- FDA Inspection 729349 - 2011-06-13
- FDA Inspection 713061 - 2011-03-08
- FDA Inspection 629365 - 2009-11-19
- FDA Inspection 582091 - 2009-05-08
- FDA Inspection 582090 - 2009-05-08
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