FDA Inspection
Synthes (USA) Products LLCSynthes (USA) Products LLC – FDA Inspection, Apr 27, 2009
Record Details
This FDA Inspection record concerns Synthes (USA) Products LLC, with an inspection on April 27, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Synthes (USA) Products LLC
- Inspection Date
- April 27, 2009
- Product Type
- Devices
View Company Profile
ID · f3b6282d-7e11-44a8-8b85-df09fd1b98b8
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 583439
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Synthes (USA) Products LLC
6| Date | Classification | Office | Project area |
|---|---|---|---|
| October 20, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 17, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 13, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 25, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 29, 2010 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Synthes (USA) Products LLC
- FDA Inspection 1029323 - 2017-10-20
- FDA Inspection 1032557 - 2017-10-17
- FDA Inspection 1028729 - 2017-10-13
- FDA Inspection 1083832 - 2017-09-25
- FDA Inspection 695834 - 2010-10-29
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