FDA inspection
Mizuho Corporation Gosen Factory: FDA inspection ending Sep 3, 2015
FDA inspection 946034 · Voluntary Action Indicated (VAI) · Gosen
Key facts
| Inspection ID | 946034 |
|---|---|
| Firm | Mizuho Corporation Gosen Factory |
| FEI number | 3009504761 |
| Address | 3631-14, Akomi |
| City | Gosen |
| Country | Japan |
| Fiscal year | 2015 |
| Inspection end date | Sep 3, 2015 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None 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