FDA inspection
Goodman Company, Ltd.: FDA inspection ending Apr 10, 2025
FDA inspection 1267718 · Nagoya
Key facts
| Inspection ID | 1267718 |
|---|---|
| Firm | Goodman Company, Ltd. |
| FEI number | 1000533027 |
| Address | 108, Fujigaoka; Meito |
| City | Nagoya |
| Fiscal year | 2025 |
| Inspection end date | Apr 10, 2025 |
| Project area | Product Evaluation: Medical 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