FDA inspection
KOFU FACTORY OF TERUMO CORP.: FDA inspection ending Jul 25, 2018
FDA inspection 1061387 · Voluntary Action Indicated (VAI) · Nakakoma-Gun
Key facts
| Inspection ID | 1061387 |
|---|---|
| Firm | KOFU FACTORY OF TERUMO CORP. |
| FEI number | 3003752255 |
| Address | 1727-1, Tsuijiarai; Showa-Cho |
| City | Nakakoma-Gun |
| Fiscal year | 2018 |
| Inspection end date | Jul 25, 2018 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | New Drug Evaluation |
| 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