FDA Inspection 667934 — Bayer AG
The FDA completed an inspection of Bayer AG on May 27, 2010 in Wuppertal. 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
- May 27, 2010
- Fiscal Year
- 2010
- Product Type
- Drugs
- Project Area
- Bioresearch Monitoring
- Location
- Wuppertal (Germany)
Additional Details
Postmarket Adverse Drug Experience (PADE)