FDA Inspection 1161093 — Simtra Deutschland GmbH
The FDA completed an inspection of Simtra Deutschland GmbH on Jan 29, 2020 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
- Jan 29, 2020
- Fiscal Year
- 2020
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Halle (Westf.) (Germany)
Additional Details
Mutual Recognition Agreement (MRA)