Oscor Caribe, LLC
Oscor Caribe, LLC has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 0 compliance actions on record.
- Latest inspection
- Aug 22, 2025 · NAI
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Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 4, 2026 (checked Nov 8, 2026, unchanged) | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 0 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
| Inspections | 6 | Nov 10, 2026 | Newest record Nov 5, 2026 | Current |
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Aug 22, 2025 | Santo Domingo, Dominican Republic (The) | Devices | No Action Indicated (NAI) | 3004785273 |
| Jan 18, 2023 | Santo Domingo, Dominican Republic (The) | Devices | No Action Indicated (NAI) | 3004785273 |
| Dec 11, 2019 | Santo Domingo, Dominican Republic (The) | Devices | No Action Indicated (NAI) | 3004785273 |
| Jul 25, 2013 | Santo Domingo, Dominican Republic (The) | Devices | Voluntary Action Indicated (VAI) | 3004785273 |
| Aug 19, 2011 | Santo Domingo, Dominican Republic (The) | Devices | Voluntary Action Indicated (VAI) | 3004785273 |
| Jun 25, 2009 | Santo Domingo, Dominican Republic (The) | Devices | Voluntary Action Indicated (VAI) | 3004785273 |
FDA-Inspected Facilities
| Facility | Location | Inspections | Latest |
|---|---|---|---|
| FEI 3004785273 | Santo Domingo, Dominican Republic (The) | 6 | Aug 22, 2025 |