FDA Inspection 932059 — Serumwerk Bernburg AG
The FDA completed an inspection of Serumwerk Bernburg AG on Jun 5, 2015 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: Drugs.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Jun 5, 2015
- Fiscal Year
- 2015
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Bernburg (Saale) (Germany)