FDA Inspection
Stryker CorporationStryker Corporation – FDA Inspection, Jun 18, 2012
Record Details
This FDA Inspection record concerns Stryker Corporation, with an inspection on June 18, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Stryker Corporation
- Inspection Date
- June 18, 2012
- Product Type
- Devices
View Company Profile
ID · f25e380b-2138-4f26-b3b2-360f04e543dc
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 791489
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Stryker Corporation
5| Date | Classification | Office | Project area |
|---|---|---|---|
| January 7, 2016 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| September 13, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 9, 2012 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 24, 2010 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| May 14, 2009 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Stryker Corporation
- FDA Inspection 959090 - 2016-01-07
- FDA Inspection 850254 - 2013-09-13
- FDA Inspection 806763 - 2012-11-09
- FDA Inspection 682479 - 2010-09-24
- FDA Inspection 583137 - 2009-05-14
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