FDA inspection
Dexcowin Co. Ltd.: FDA inspection ending Mar 26, 2015
FDA inspection 921780 · Official Action Indicated (OAI) · Geumcheon
Key facts
| Inspection ID | 921780 |
|---|---|
| Firm | Dexcowin Co. Ltd. |
| FEI number | 3007065358 |
| Address | # 606 Woolim Lions Valley Ii |
| City | Geumcheon |
| Country | Korea (the Republic of) |
| Fiscal year | 2015 |
| Inspection end date | Mar 26, 2015 |
| Classification | Official Action Indicated (OAI) |
| Project area | Postmarket Assurance: 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