FDA inspection
Toyobo Co. Ltd.: FDA inspection ending Jan 23, 2018
FDA inspection 1039008 · Voluntary Action Indicated (VAI) · Otsu
Key facts
| Inspection ID | 1039008 |
|---|---|
| Firm | Toyobo Co. Ltd. |
| FEI number | 1000251214 |
| Address | Toyobo (Kabu) Sogokenkyusho, 2 Chome Sogokenkyusho; Katata |
| City | Otsu |
| Fiscal year | 2018 |
| Inspection end date | Jan 23, 2018 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | New Drug Evaluation |
| 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