FDA inspection
Goodman Co., Ltd. Goodman Research Center / Goodman Medical Innovation Center: FDA inspection ending May 15, 2025
FDA inspection 1274186 · No Action Indicated (NAI) · Seto
Key facts
| Inspection ID | 1274186 |
|---|---|
| Firm | Goodman Co., Ltd. Goodman Research Center / Goodman Medical Innovation Center |
| FEI number | 3011826338 |
| Address | 276 1 Idogane Cho Seto Sh, Idogane-Cho |
| City | Seto |
| Country | Japan |
| Fiscal year | 2025 |
| Inspection end date | May 15, 2025 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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