FDA inspection
Nihon Kohden Tomioka Corporation: FDA inspection ending Dec 15, 2017
FDA inspection 1089707 · No Action Indicated (NAI) · Tomioka
Key facts
| Inspection ID | 1089707 |
|---|---|
| Firm | Nihon Kohden Tomioka Corporation |
| FEI number | 3002807739 |
| Address | 1-1, Tajino |
| City | Tomioka |
| Fiscal year | 2018 |
| Inspection end date | Dec 15, 2017 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Medical Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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