FDA inspection
Genoray Co Ltd: FDA inspection ending May 31, 2011
FDA inspection 733281 · Voluntary Action Indicated (VAI) · Seongnam
Key facts
| Inspection ID | 733281 |
|---|---|
| Firm | Genoray Co Ltd |
| FEI number | 3005843418 |
| Address | 512, 560, Dunchon-Daero, Jungwon-Gu |
| City | Seongnam |
| Country | Korea (the Republic of) |
| Fiscal year | 2011 |
| Inspection end date | May 31, 2011 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Radiation Control and Health Safety Act |
| 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