FDA Inspection 905879 — Bayer AG

Bayer AG — FEI 3002806462

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

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