FDA Inspection 1040866 — Serumwerk Bernburg AG
The FDA completed an inspection of Serumwerk Bernburg AG on Jan 12, 2018 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
- Jan 12, 2018
- Fiscal Year
- 2018
- Product Type
- Veterinary
- Project Area
- Monitoring of Marketed Animal Drugs, Feed, and Devices
- Location
- Bernburg (Saale) (Germany)