FDA Inspection 948310 — 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 November 5, 2015 in Weimar. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 5, 2015
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Weimar (Germany)