FDA Inspection 869792 — Stryker Corporation
The FDA completed an inspection of Stryker Corporation on Mar 12, 2014 in Minnetonka, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Mar 12, 2014
- Fiscal Year
- 2014
- Product Type
- Biologics
- Project Area
- Human Cellular, Tissue, and Gene Therapies
- Location
- Minnetonka, MN (United States)