FDA Inspection 735246 — B. Braun Avitum AG

B. Braun Avitum AG — FEI 3002879653

The FDA completed an inspection of B. Braun Avitum AG on June 17, 2011 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
June 17, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Melsungen (Germany)