FDA Inspection 1306752 — Antoinette Neylon
The FDA completed an inspection of Antoinette Neylon on Feb 19, 2026 in Massy. 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
- Feb 19, 2026
- Fiscal Year
- 2026
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Massy (France)
Additional details
Clinical Investigator (CI)