FDA inspection
HOYA Corporation PENTAX Miyagi Factory: FDA inspection ending Feb 21, 2006
FDA inspection 416650 · No Action Indicated (NAI) · Kurihara
Key facts
| Inspection ID | 416650 |
|---|---|
| Firm | HOYA Corporation PENTAX Miyagi Factory |
| FEI number | 3003782610 |
| Address | Aza-Shimomiyano 30-2, Tsukidate |
| City | Kurihara |
| Fiscal year | 2006 |
| Inspection end date | Feb 21, 2006 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: 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