Dexcowin Co., Ltd.
Dexcowin Co., Ltd. has 0 FDA recalls, 5 inspections, 5 510(k) clearances and 2 compliance actions on record.
- Latest inspection
- Feb 23, 2023 · VAI
- Latest 510(k)
- Oct 26, 2017
Reviewing Dexcowin Co., Ltd. as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.
Or get Dexcowin Co., Ltd.'s full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site, in Claude, Cursor or ChatGPT.
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Oct 23, 2026 | Not stated | Current |
| 510(k) clearances | 5 | Oct 4, 2026 | Not stated | Current |
| Inspections | 5 | Oct 25, 2026 | Not stated | Current |
| Compliance actions | 2 | Oct 23, 2026 | Not stated | Current |
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Feb 23, 2023 | Geumcheon, Korea (The Republic Of) | Devices | Voluntary Action Indicated (VAI) | 3007065358 |
| Jun 6, 2019 | Geumcheon, Korea (The Republic Of) | Devices | No Action Indicated (NAI) | 3007065358 |
| Aug 31, 2017 | Geumcheon, Korea (The Republic Of) | Devices | Official Action Indicated (OAI) | 3007065358 |
| Mar 26, 2015 | Geumcheon, Korea (The Republic Of) | Devices | Official Action Indicated (OAI) | 3007065358 |
| Jun 3, 2011 | Geumcheon, Korea (The Republic Of) | Devices | Voluntary Action Indicated (VAI) | 3007065358 |