FDA Inspection 1193872 — Bionen S.r.l.

Bionen S.r.l. — FEI 3008617703

The FDA completed an inspection of Bionen S.r.l. on December 7, 2022 in Florence. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 7, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Florence (Italy)