FDA Inspection 1328670 — B. Braun Avitum Saxonia GmbH

B. Braun Avitum Saxonia GmbH — FEI 3004201412

The FDA completed an inspection of B. Braun Avitum Saxonia GmbH on Jul 2, 2026 in Radeberg. 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
Jul 2, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Radeberg (Germany)