Unimed S.A.
FDA Regulatory Profile
Unimed S.A. has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record.
- Latest inspection
- May 27, 2025 · NAI
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Summary
Record counts and when each FDA source was last refreshed
| 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 | 1 | Nov 11, 2026 | Newest record Nov 5, 2026 | Current |
|---|
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
|---|
Related names
| Name | Recalls | 510(k) | Inspections | Compliance | Most recent recall |
|---|
Un-I-Med
Same company group | 0 | 2 | 0 | 0 | — |
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
|---|
| May 27, 2025 | Ecublens Vd, Switzerland | Devices | No Action Indicated (NAI) | 5638 |
NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.
FDA-Inspected Facilities
| Facility | Location | Inspections | Latest |
|---|
| FEI 5638 | Ecublens Vd, Switzerland | 1 | May 27, 2025 |