Drug factory · FDA FEI 3002806998
Finorga
AVENUE DU LAC, Mourenx, France
Problems found, fixed voluntarily at FDA's last inspection, Nov 24, 2023.
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 2013: 2 with no problems, 2 with problems fixed voluntarily, 0 with FDA action.
What it does, for whom
| Drug | Role | For | NDC |
|---|---|---|---|
| Encorafenib | Makes the active ingredient | Array BioPharma Inc. | 70255-050 |
FDA inspection history
| Ended | Result | Program | Problems noted |
|---|---|---|---|
| Nov 24, 2023 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| Sep 20, 2019 | No problems found | Drug Quality Assurance | — |
| Sep 23, 2016 | No problems found | Drug Quality Assurance | — |
| Dec 13, 2013 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
Registered with FDA for: analysis; api manufacture.