# FDA Inspection 965787 - Stryker GmbH - February 25, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/stryker-gmbh/df359d01-411b-41dd-8b82-aedbbe7f2f91
Source feed: FDA_Inspections

> FDA Inspection 965787 for Stryker GmbH on February 25, 2016. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 965787
- Company Name: Stryker GmbH
- Inspection Date: 2016-02-25
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1263754 - 2025-03-27](https://www.globalkeysolutions.net/records/fda_inspections/stryker-gmbh/b8060c9e-bf75-4183-9841-1240bfb60b53)
- [FDA Inspection 1263754 - 2025-03-27](https://www.globalkeysolutions.net/records/fda_inspections/stryker-gmbh/7557539d-337a-4d82-b8b9-6f04cdb2f644)
- [FDA Inspection 1263754 - 2025-03-27](https://www.globalkeysolutions.net/records/fda_inspections/stryker-gmbh/a8194ede-eb2d-4878-a016-f6cf4c3206bf)
- [FDA Inspection 1263754 - 2025-03-27](https://www.globalkeysolutions.net/records/fda_inspections/stryker-gmbh/31130694-c3d2-4bd7-b87b-05f94cb9802b)
- [FDA Inspection 750625 - 2011-09-22](https://www.globalkeysolutions.net/records/fda_inspections/stryker-gmbh/a150895b-a254-4c93-9b6e-36b168734ae3)

Company: https://www.globalkeysolutions.net/companies/stryker-gmbh/c74b50c4-3566-425d-9331-7fb21b736586

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7