FDA Inspection 1056958 — Simtra Deutschland GmbH
The FDA completed an inspection of Simtra Deutschland GmbH on Jun 14, 2018 in Halle (Westf.). 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 14, 2018
- Fiscal Year
- 2018
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Halle (Westf.) (Germany)