FDA Inspection 944344 — Biomatlante

Biomatlante — FEI 3002673655

The FDA completed an inspection of Biomatlante on Sep 17, 2015 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
Sep 17, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Vigneux De Bretagne (France)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.