FDA Inspection 841970 — Sanofi-Aventis Deutschland GmbH
The FDA completed an inspection of Sanofi-Aventis Deutschland GmbH on Jul 2, 2013 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: Devices.
Inspection details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Jul 2, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Frankfurt Am Main (Germany)