FDA inspection
Mitsubishi Tanabe Pharma Factory Ltd.: FDA inspection ending Dec 11, 2015
FDA inspection 950893 · Voluntary Action Indicated (VAI) · San'Yoonoda
Key facts
| Inspection ID | 950893 |
|---|---|
| Firm | Mitsubishi Tanabe Pharma Factory Ltd. |
| FEI number | 3002808316 |
| Address | 7473-2, Danhigashi |
| City | San'Yoonoda |
| Country | Japan |
| Fiscal year | 2016 |
| Inspection end date | Dec 11, 2015 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- 1–9 Citations
- 1–9 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