FDA inspection
Fujifilm Healthcare Americas Corporation: FDA inspection ending May 2, 2016
FDA inspection 975171 · Voluntary Action Indicated (VAI) · Greenville, SC
Key facts
| Inspection ID | 975171 |
|---|---|
| Firm | Fujifilm Healthcare Americas Corporation |
| FEI number | 3019837913 |
| Address | 204 Westfield St |
| City | Greenville |
| State | SC |
| ZIP | 29601 |
| Country | United States |
| Fiscal year | 2016 |
| Inspection end date | May 2, 2016 |
| 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