FDA Inspection 586860 — Stryker Spine
The FDA completed an inspection of Stryker Spine on May 28, 2009 in Cestas, Nouvelle-Aquitaine. 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
- May 28, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Cestas, Nouvelle-Aquitaine (France)