FDA inspection
Rohto Pharmaceutical Co., Ltd. (Ueno Plant): FDA inspection ending Nov 20, 2012
FDA inspection 812116 · Voluntary Action Indicated (VAI) · Iga
Key facts
| Inspection ID | 812116 |
|---|---|
| Firm | Rohto Pharmaceutical Co., Ltd. (Ueno Plant) |
| FEI number | 3003722237 |
| Address | 7 Chome 3 Ueno Technocenter, Yumegaoka |
| City | Iga |
| Country | Japan |
| Fiscal year | 2013 |
| Inspection end date | Nov 20, 2012 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None 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