FDA Inspection 1263642 — Dyn'r
The FDA completed an inspection of Dyn'r on Feb 6, 2025 in Aix-En-Provence. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Feb 6, 2025
- Fiscal Year
- 2025
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Aix-En-Provence (France)