FDA Inspection
Synthes, Inc.Synthes, Inc. – FDA Inspection, Apr 27, 2009
Record Details
This FDA Inspection record concerns Synthes, Inc., with an inspection on April 27, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Synthes, Inc.
- Inspection Date
- April 27, 2009
- Product Type
- Devices
View Company Profile
ID · 7a7a89d7-4ea5-4f5b-ba05-5adf357be5fb
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 581756
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Synthes, Inc.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| November 13, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 16, 2013 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| October 19, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 15, 2011 | OAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| October 8, 2009 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Synthes, Inc.
- FDA Inspection 859106 - 2013-11-13
- FDA Inspection 831886 - 2013-05-16
- FDA Inspection 806156 - 2012-10-19
- FDA Inspection 732622 - 2011-09-15
- FDA Inspection 620039 - 2009-10-08
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