FDA inspection
Tochigi Seiko Kk: FDA inspection ending Dec 17, 2015
FDA inspection 956228 · No Action Indicated (NAI) · Tochigi
Key facts
| Inspection ID | 956228 |
|---|---|
| Firm | Tochigi Seiko Kk |
| FEI number | 3004521048 |
| Address | 2 Chome 1-5, Hirayanagi-Machi |
| City | Tochigi |
| Country | Japan |
| Fiscal year | 2016 |
| Inspection end date | Dec 17, 2015 |
| 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