FDA inspection
Menicon Co., Ltd.: FDA inspection ending Jul 22, 2005
FDA inspection 392721 · Voluntary Action Indicated (VAI) · Nagoya
Key facts
| Inspection ID | 392721 |
|---|---|
| Firm | Menicon Co., Ltd. |
| FEI number | 1000188353 |
| Address | 3 Chome 21-19, Naka-Ku |
| City | Nagoya |
| Fiscal year | 2005 |
| Inspection end date | Jul 22, 2005 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med 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