FDA inspection
Genemax Medical Products Industry Corp.: FDA inspection ending Mar 17, 2015
FDA inspection 920198 · No Action Indicated (NAI) · Taichung
Key facts
| Inspection ID | 920198 |
|---|---|
| Firm | Genemax Medical Products Industry Corp. |
| FEI number | 3003123807 |
| Address | No. 86, Lane 226, Tai Ming Rd, Wu Jih District |
| City | Taichung |
| Country | Taiwan |
| Fiscal year | 2015 |
| Inspection end date | Mar 17, 2015 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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