FDA inspection
FUJIFILM Healthcare Americas Corporation: FDA inspection ending Nov 3, 2004
FDA inspection 352960 · Voluntary Action Indicated (VAI) · Lexington, MA
Key facts
| Inspection ID | 352960 |
|---|---|
| Firm | FUJIFILM Healthcare Americas Corporation |
| FEI number | 1000513161 |
| Address | 81 Hartwell Ave Ste 300 |
| City | Lexington |
| State | MA |
| ZIP | 02421-3160 |
| Fiscal year | 2005 |
| Inspection end date | Nov 3, 2004 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med 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
- 10–99 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