Intercos Europe SpA
Intercos Europe SpA has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 1 compliance action on record.
- Latest inspection
- Nov 29, 2024 · VAI
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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 | 5 | Nov 8, 2026 | Newest record Oct 28, 2026 | Current |
| Compliance actions | 1 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Nov 29, 2024 | Dovera, Italy | Drugs | Voluntary Action Indicated (VAI) | 3005291719 |
| Mar 15, 2024 | Agrate Brianza, Italy | Drugs | Official Action Indicated (OAI) | 1000181428 |
| Sep 11, 2019 | Dovera, Italy | Drugs | No Action Indicated (NAI) | 3005291719 |
| Jun 24, 2016 | Dovera, Italy | Drugs | Voluntary Action Indicated (VAI) | 3005291719 |
| Feb 13, 2015 | Agrate Brianza, Italy | Drugs | Voluntary Action Indicated (VAI) | 1000181428 |
FDA-Inspected Facilities
| Facility | Location | Inspections | Latest |
|---|---|---|---|
| FEI 3005291719 | Dovera, Italy | 3 | Nov 29, 2024 |
| FEI 1000181428 | Agrate Brianza, Italy | 2 | Mar 15, 2024 |