FDA inspection
Goodman Co., Ltd: FDA inspection ending Jan 25, 2024
FDA inspection 1227869 · Voluntary Action Indicated (VAI) · Nagoya
Key facts
| Inspection ID | 1227869 |
|---|---|
| Firm | Goodman Co., Ltd |
| FEI number | 3007835716 |
| Address | 5f Kdx Nagoya Sakae Building, 4-5-3 Sakae, Naka-Ku, Sakae; Naka |
| City | Nagoya |
| Country | Japan |
| Fiscal year | 2024 |
| Inspection end date | Jan 25, 2024 |
| 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