FDA Inspection 802508 — Daiichi Sankyo Europe GmbH

Daiichi Sankyo Europe GmbH — FEI 3003282622

The FDA completed an inspection of Daiichi Sankyo Europe GmbH on September 20, 2012 in Pfaffenhofen A.D.Ilm. 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
September 20, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Pfaffenhofen A.D.Ilm (Germany)