FDA Inspection 1126224 — Bayer AG

Bayer AG — FEI 3002808084

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

Additional details

Mutual Recognition Agreement (MRA)

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