FDA Inspection 636510 — Bayer Weimar GmbH und Co. KG
The FDA completed an inspection of Bayer Weimar GmbH und Co. KG on December 4, 2009 in Weimar. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- December 4, 2009
- Fiscal Year
- 2010
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Weimar (Germany)