FDA Inspection 1072256 — Stryker Manufacturing S. De R.L. De C.V.
The FDA completed an inspection of Stryker Manufacturing S. De R.L. De C.V. on Oct 24, 2018 in La Masa Tijuana. 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
- Oct 24, 2018
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- La Masa Tijuana (Mexico)