FDA Inspection 1263754 — Stryker GmbH

Stryker GmbH — FEI 3002807830

The FDA completed an inspection of Stryker GmbH on March 27, 2025 in Selzach. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 27, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Selzach (Switzerland)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures