FDA inspection
FUJIFILM Corporation Medical Systems Research & Development Center Kashiwa: FDA inspection ending Dec 21, 2017
FDA inspection 1037713 · Voluntary Action Indicated (VAI) · Kashiwa
Key facts
| Inspection ID | 1037713 |
|---|---|
| Firm | FUJIFILM Corporation Medical Systems Research & Development Center Kashiwa |
| FEI number | 3018423337 |
| Address | 2-1, Shintoyofuta |
| City | Kashiwa |
| Country | Japan |
| Fiscal year | 2018 |
| Inspection end date | Dec 21, 2017 |
| 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