FDA inspection
FUJIFILM Healthcare Americas Corporation: FDA inspection ending Nov 8, 2017
FDA inspection 1032528 · No Action Indicated (NAI) · Durham, NC
Key facts
| Inspection ID | 1032528 |
|---|---|
| Firm | FUJIFILM Healthcare Americas Corporation |
| FEI number | 3004972322 |
| Address | 3020 Carrington Mill Blvd Ste 500 |
| City | Durham |
| State | NC |
| ZIP | 27709 |
| Country | United States |
| Fiscal year | 2018 |
| Inspection end date | Nov 8, 2017 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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