FDA inspection
Menicon Kakamigahara Plant: FDA inspection ending Aug 30, 2018
FDA inspection 1126514 · Voluntary Action Indicated (VAI) · Kakamigahara
Key facts
| Inspection ID | 1126514 |
|---|---|
| Firm | Menicon Kakamigahara Plant |
| FEI number | 3014768085 |
| Address | 3 21-3, Technoplaza |
| City | Kakamigahara |
| Fiscal year | 2018 |
| Inspection end date | Aug 30, 2018 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Medical 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