FDA Inspection 1051187 — SpineGuard, SA
The FDA completed an inspection of SpineGuard, SA on Mar 29, 2018 in Vincennes. 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
- Mar 29, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Vincennes (France)