FDA Inspection 649526 — Daiichi Sankyo Europe GmbH
The FDA completed an inspection of Daiichi Sankyo Europe GmbH on Jan 29, 2010 in Pfaffenhofen A.D.Ilm. 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
- Jan 29, 2010
- Fiscal Year
- 2010
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Pfaffenhofen A.D.Ilm (Germany)