FDA Inspection 905879 — Bayer AG

Bayer AG — FEI 3002806462

The FDA completed an inspection of Bayer AG on November 14, 2014 in Leverkusen. 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
November 14, 2014
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Leverkusen (Germany)