FDA inspection
Menicon Nect Co., Ltd., Gujo Plant: FDA inspection ending Dec 11, 2015
FDA inspection 954844 · No Action Indicated (NAI) · Gujo
Key facts
| Inspection ID | 954844 |
|---|---|
| Firm | Menicon Nect Co., Ltd., Gujo Plant |
| FEI number | 3010607087 |
| Address | 3 Chome 15, Hachimanchogo-Cho |
| City | Gujo |
| Country | Japan |
| Fiscal year | 2016 |
| Inspection end date | Dec 11, 2015 |
| 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