FDA inspection
Dexcowin Co. Ltd.: FDA inspection ending Jun 6, 2019
FDA inspection 1101231 · No Action Indicated (NAI) · Geumcheon
Key facts
| Inspection ID | 1101231 |
|---|---|
| Firm | Dexcowin Co. Ltd. |
| FEI number | 3007065358 |
| Address | # 606 Woolim Lions Valley Ii |
| City | Geumcheon |
| Country | Korea (the Republic of) |
| Fiscal year | 2019 |
| Inspection end date | Jun 6, 2019 |
| 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