FDA Inspection
Stryker GmbHStryker GmbH – FDA Inspection, Mar 27, 2025
Record Details
This FDA Inspection record concerns Stryker GmbH, with an inspection on March 27, 2025, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
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ID · b8060c9e-bf75-4183-9841-1240bfb60b53
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1263754
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Medical Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.100(a)Lack of or inadequate procedures
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Other FDA inspections of Stryker GmbH
3| Date | Classification | Office | Project area |
|---|---|---|---|
| February 25, 2016 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 22, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 6, 2008 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Stryker GmbH
- FDA Inspection 965787 - 2016-02-25
- FDA Inspection 750625 - 2011-09-22
- FDA Inspection 551172 - 2008-11-06
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