FDA Inspection 1316972 — B. Braun Avitum AG

B. Braun Avitum AG — FEI 3002879653

The FDA completed an inspection of B. Braun Avitum AG on April 23, 2026 in Melsungen. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 23, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Melsungen (Germany)