FDA Inspection 1269118 — LISI MEDICAL FASTENERS
The FDA completed an inspection of LISI MEDICAL FASTENERS on Apr 16, 2025 in Neyron. 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
- Apr 16, 2025
- Fiscal Year
- 2025
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Neyron (France)