FDA inspection
AOMORI OLYMPUS CO., LTD. Kuroishi Site: FDA inspection ending Mar 2, 2016
FDA inspection 960600 · No Action Indicated (NAI) · Kuroishi
Key facts
| Inspection ID | 960600 |
|---|---|
| Firm | AOMORI OLYMPUS CO., LTD. Kuroishi Site |
| FEI number | 3003995201 |
| Address | 2 Chome 248-1, Okkonoki |
| City | Kuroishi |
| Country | Japan |
| Fiscal year | 2016 |
| Inspection end date | Mar 2, 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