FDA inspection
SUZUKEN CO., LTD. OGUCHI CENTER: FDA inspection ending Jun 17, 2015
FDA inspection 933588 · Voluntary Action Indicated (VAI) · Niwa-Gun
Key facts
| Inspection ID | 933588 |
|---|---|
| Firm | SUZUKEN CO., LTD. OGUCHI CENTER |
| FEI number | 3006540105 |
| Address | 1 Chome 58-1, Totsubo; Oguchi-Cho |
| City | Niwa-Gun |
| Country | Japan |
| Fiscal year | 2015 |
| Inspection end date | Jun 17, 2015 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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