FDA Inspection
Creaspine SASCreaspine SAS – FDA Inspection, Oct 18, 2012
Record Details
This FDA Inspection record concerns Creaspine SAS, with an inspection on October 18, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Creaspine SAS
- Inspection Date
- October 18, 2012
- Product Type
- Devices
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ID · 2bee570d-d71a-44e9-84c8-57cf4c587223
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 804960
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.184DHR - not or inadequately maintained
- 21 CFR 820.150Lack of or inadequate procedures for storage.
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Other FDA inspections of Creaspine SAS
2| Date | Classification | Office | Project area |
|---|---|---|---|
| September 22, 2011 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 30, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Creaspine SAS
- FDA Inspection 749556 - 2011-09-22
- FDA Inspection 612912 - 2009-07-30
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