FDA inspection
Daiichi Sankyo Propharma Co., Ltd.: FDA inspection ending Jan 22, 2001
FDA inspection 67624 · No Action Indicated (NAI) · Hiratsuka
Key facts
| Inspection ID | 67624 |
|---|---|
| Firm | Daiichi Sankyo Propharma Co., Ltd. |
| FEI number | 3002808070 |
| Address | 1 Chome 12-1, Shinomiya |
| City | Hiratsuka |
| Fiscal year | 2001 |
| Inspection end date | Jan 22, 2001 |
| Classification | No Action Indicated (NAI) |
| 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