Baxter Productos Medicos, Ltda.
Baxter Productos Medicos, Ltda. has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 0 compliance actions on record.
- Latest inspection
- May 24, 2018 · NAI
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Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 0 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
| Inspections | 4 | Nov 14, 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 |
|---|---|---|---|---|
| May 24, 2018 | Cartago, Costa Rica | Devices | No Action Indicated (NAI) | 3002806588 |
| May 19, 2016 | Cartago, Costa Rica | Devices | No Action Indicated (NAI) | 3002806588 |
| May 9, 2013 | Cartago, Costa Rica | Devices | No Action Indicated (NAI) | 3002806588 |
| Jul 21, 2011 | Cartago, Costa Rica | Devices | No Action Indicated (NAI) | 3002806588 |
- NAI
- No objectionable conditions or practices were found during the inspection.
- VAI
- Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
- OAI
- Regulatory and/or administrative actions are recommended.
FDA-inspected facilities
| Facility | Location | Inspections | Latest |
|---|---|---|---|
| FEI 3002806588 | Cartago, Costa Rica | 4 | May 24, 2018 |
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