FDA Inspection 788644 — Sanofi-Aventis Deutschland GmbH
The FDA completed an inspection of Sanofi-Aventis Deutschland GmbH on Apr 30, 2012 in Frankfurt Am Main. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Apr 30, 2012
- Fiscal Year
- 2012
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Frankfurt Am Main (Germany)