FDA Inspection 1246172 — Serumwerk Bernburg AG

Serumwerk Bernburg AG — FEI 3003903447

The FDA completed an inspection of Serumwerk Bernburg AG on Jun 14, 2024 in Bernburg (Saale). The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 14, 2024
Fiscal Year
2024
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Bernburg (Saale) (Germany)