FDA Inspection 803657 — Bayer AG

Bayer AG — FEI 3002808086

The FDA completed an inspection of Bayer AG on Sep 18, 2012 in Berlin. 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
Sep 18, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Berlin (Germany)

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