FDA Inspection
Creaspine SASCreaspine SAS – FDA Inspection, Sep 22, 2011
Record Details
This FDA Inspection record concerns Creaspine SAS, with an inspection on September 22, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Creaspine SAS
- Inspection Date
- September 22, 2011
- Product Type
- Devices
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ID · 0b3d173f-2d51-4705-9b1f-de1546dd9888
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 749556
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.75(a)Lack of or inadequate process validation
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Other FDA inspections of Creaspine SAS
2| Date | Classification | Office | Project area |
|---|---|---|---|
| October 18, 2012 | 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 804960 - 2012-10-18
- FDA Inspection 612912 - 2009-07-30
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