FDA Inspection 805216 — Bayer Weimar GmbH Und Co. KG

Bayer Weimar GmbH Und Co. KG — FEI 3002808091

The FDA completed an inspection of Bayer Weimar GmbH Und Co. KG on Oct 19, 2012 in Weimar. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Oct 19, 2012
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Weimar (Germany)

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