FDA inspection
Daiichi Sankyo Europe GmbH: FDA inspection ending Jun 9, 2017
FDA inspection 1019118 · Pfaffenhofen A.D.Ilm
Key facts
| Inspection ID | 1019118 |
|---|---|
| Firm | Daiichi Sankyo Europe GmbH |
| FEI number | 3003282622 |
| Address | Luitpoldstr. 1 |
| City | Pfaffenhofen A.D.Ilm |
| Fiscal year | 2017 |
| Inspection end date | Jun 9, 2017 |
| Project area | New Drug Evaluation |
| Product type | Drugs |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data