FDA inspection
Nihon Kohden Tomioka Corporation: FDA inspection ending Jun 25, 2008
FDA inspection 530315 · No Action Indicated (NAI) · Tomioka
Key facts
| Inspection ID | 530315 |
|---|---|
| Firm | Nihon Kohden Tomioka Corporation |
| FEI number | 3002807739 |
| Address | 1-1, Tajino |
| City | Tomioka |
| Fiscal year | 2008 |
| Inspection end date | Jun 25, 2008 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Med 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