FDA inspection
Yokowo Co Ltd: FDA inspection ending Apr 13, 2017
FDA inspection 1015641 · Voluntary Action Indicated (VAI) · Tomioka
Key facts
| Inspection ID | 1015641 |
|---|---|
| Firm | Yokowo Co Ltd |
| FEI number | 3009092139 |
| Address | (Kabu) Yoko, ) Yoko Kabu ) Yoko Kabu 1112; Kanohara |
| City | Tomioka |
| Country | Japan |
| Fiscal year | 2017 |
| Inspection end date | Apr 13, 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