FDA Inspection 1297696 — Stryker Manufacturing Kalamazoo
The FDA completed an inspection of Stryker Manufacturing Kalamazoo on December 11, 2025 in Portage, MI. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- December 11, 2025
- Fiscal Year
- 2026
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Portage, MI (United States)