FDA inspection
Fukuda Denshi Co., Ltd.: FDA inspection ending Apr 10, 2025
FDA inspection 1269722 · Voluntary Action Indicated (VAI) · Bunkyo
Key facts
| Inspection ID | 1269722 |
|---|---|
| Firm | Fukuda Denshi Co., Ltd. |
| FEI number | 3002807019 |
| Address | Fukudadenshi, 3 Chome 39-4; Hongo |
| City | Bunkyo |
| Country | Japan |
| Fiscal year | 2025 |
| Inspection end date | Apr 10, 2025 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: Devices |
| Product type | Devices |
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