FDA inspection
FUJIFILM Healthcare Manufacturing Corporation Sano Office: FDA inspection ending Sep 10, 2019
FDA inspection 1114409 · Official Action Indicated (OAI) · Sano
Key facts
| Inspection ID | 1114409 |
|---|---|
| Firm | FUJIFILM Healthcare Manufacturing Corporation Sano Office |
| FEI number | 3002808127 |
| Address | 700, Konaka-Cho |
| City | Sano |
| Country | Japan |
| Fiscal year | 2019 |
| Inspection end date | Sep 10, 2019 |
| Classification | Official Action Indicated (OAI) |
| 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