FDA Inspection 1059195 — Stryker Corporation
The FDA completed an inspection of Stryker Corporation on Jun 11, 2018 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
- Jun 11, 2018
- Fiscal Year
- 2018
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Minnetonka, MN (United States)