FDA Inspection
STRYKER IRELAND OSTEONICSSTRYKER IRELAND OSTEONICS – FDA Inspection, Jan 15, 2015
Record Details
This FDA Inspection record concerns STRYKER IRELAND OSTEONICS, with an inspection on January 15, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- STRYKER IRELAND OSTEONICS
- Inspection Date
- January 15, 2015
- Product Type
- Devices
View Company Profile
ID · d77895f7-265d-4eb5-b900-012ac5cd9694
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 909984
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of STRYKER IRELAND OSTEONICS
3| Date | Classification | Office | Project area |
|---|---|---|---|
| February 2, 2017 | Not classified | Office of Inspections and Investigations | |
| July 28, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 21, 2009 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for STRYKER IRELAND OSTEONICS
- FDA Inspection 1002039 - 2017-02-02
- FDA Inspection 744854 - 2011-07-28
- FDA Inspection 590920 - 2009-05-21
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