FDA inspection
Hoya Corporation - Pentax Life Division: FDA inspection ending Sep 7, 2018
FDA inspection 1131698 · Voluntary Action Indicated (VAI) · Akishima
Key facts
| Inspection ID | 1131698 |
|---|---|
| Firm | Hoya Corporation - Pentax Life Division |
| FEI number | 3008185830 |
| Address | 1 Chome 1-110, Tsutsujigaoka |
| City | Akishima |
| Fiscal year | 2018 |
| Inspection end date | Sep 7, 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