FDA Inspection 933399 — Sanofi-Aventis Deutschland GmbH
The FDA completed an inspection of Sanofi-Aventis Deutschland GmbH on Jun 26, 2015 in Frankfurt Am Main. 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 26, 2015
- Fiscal Year
- 2015
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Frankfurt Am Main (Germany)