FDA Inspection 1126224 — Bayer AG

Bayer AG — FEI 3002808084

The FDA completed an inspection of Bayer AG on October 10, 2019 in Bergkamen. 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
October 10, 2019
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Bergkamen (Germany)

Additional Details

Mutual Recognition Agreement (MRA)