FDA Inspection 750625 — Stryker GmbH
The FDA completed an inspection of Stryker GmbH on Sep 22, 2011 in Selzach. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Sep 22, 2011
- Fiscal Year
- 2011
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Selzach (Switzerland)