FDA inspection
HOYA Corporation PENTAX Miyagi Factory: FDA inspection ending Dec 16, 2010
FDA inspection 705556 · Voluntary Action Indicated (VAI) · Kurihara
Key facts
| Inspection ID | 705556 |
|---|---|
| Firm | HOYA Corporation PENTAX Miyagi Factory |
| FEI number | 3003782610 |
| Address | Aza-Shimomiyano 30-2, Tsukidate |
| City | Kurihara |
| Country | Japan |
| Fiscal year | 2011 |
| Inspection end date | Dec 16, 2010 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- 1–9 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