FDA Inspection 905792 — LDR Medical
The FDA completed an inspection of LDR Medical on Dec 4, 2014 in Sainte-Savine Aube. 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
- Dec 4, 2014
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Project Evaluation: Devices
- Location
- Sainte-Savine Aube (France)
Additional details
Postmarket Audit Inspections