FDA inspection
Menicon Co., Ltd.: FDA inspection ending Aug 27, 2007
FDA inspection 488208 · No Action Indicated (NAI) · Nagoya
Key facts
| Inspection ID | 488208 |
|---|---|
| Firm | Menicon Co., Ltd. |
| FEI number | 1000188353 |
| Address | 3 Chome 21-19, Naka-Ku |
| City | Nagoya |
| Fiscal year | 2007 |
| Inspection end date | Aug 27, 2007 |
| Classification | No Action Indicated (NAI) |
| Project area | Product Evaluation: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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