FDA Inspection 1078421 — Biomatlante
The FDA completed an inspection of Biomatlante on Nov 16, 2018 in Vigneux De Bretagne. 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
- Nov 16, 2018
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Vigneux De Bretagne (France)