Drug factory · FDA FEI 3002808250
Cerbios-Pharma SA
Via Figino 6, Barbengo/Lugano, Switzerland
Problems found, fixed voluntarily at FDA's last inspection, Mar 7, 2024.
Voluntary Action Indicated: inspectors found problems, but not serious enough for FDA to take action. The company is expected to fix them.
4 drug inspections on record since 2010: 3 with no problems, 1 with problems fixed voluntarily, 0 with FDA action.
What it does, for whom
| Drug | Role | For | NDC |
|---|---|---|---|
| Leucovorin | Makes the active ingredient | Hikma Pharmaceuticals USA Inc. | 0054-4496, 0054-4497, 0054-4498 +2 |
FDA inspection history
| Ended | Result | Program | Problems noted |
|---|---|---|---|
| Mar 7, 2024 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| Apr 27, 2018 | No problems found | Drug Quality Assurance | — |
| Feb 20, 2014 | No problems found | Drug Quality Assurance | — |
| Sep 30, 2010 | No problems found | Drug Quality Assurance | — |
Registered with FDA for: analysis; api manufacture.