FDA inspection
Unisis Corp.: FDA inspection ending Jan 23, 2020
FDA inspection 1116325 · Voluntary Action Indicated (VAI) · Koshigaya
Key facts
| Inspection ID | 1116325 |
|---|---|
| Firm | Unisis Corp. |
| FEI number | 3003803331 |
| Address | Koshigaya City, Saitama, 2675-1; Nishikata |
| City | Koshigaya |
| Country | Japan |
| Fiscal year | 2020 |
| Inspection end date | Jan 23, 2020 |
| 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