FDA Inspection 987428 — Siegfried Hameln GmbH
The FDA completed an inspection of Siegfried Hameln GmbH on Jul 1, 2016 in Hameln. 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
- Jul 1, 2016
- Fiscal Year
- 2016
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Hameln (Germany)