FDA inspection
Tokyo Boeki Medisys, Inc.: FDA inspection ending Mar 24, 2017
FDA inspection 1009378 · Voluntary Action Indicated (VAI) · Hino
Key facts
| Inspection ID | 1009378 |
|---|---|
| Firm | Tokyo Boeki Medisys, Inc. |
| FEI number | 3004378326 |
| Address | 1 Chome 14-21, Higashitoyoda |
| City | Hino |
| Country | Japan |
| Fiscal year | 2017 |
| Inspection end date | Mar 24, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
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