FDA inspection
Asahi Kasei Medical MT Co., Okatomi Plant: FDA inspection ending Mar 25, 2016
FDA inspection 974282 · No Action Indicated (NAI) · Nobeoka
Key facts
| Inspection ID | 974282 |
|---|---|
| Firm | Asahi Kasei Medical MT Co., Okatomi Plant |
| FEI number | 3007340888 |
| Address | 5 Chome 4960, Nakagawara-Cho |
| City | Nobeoka |
| Country | Japan |
| Fiscal year | 2016 |
| Inspection end date | Mar 25, 2016 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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