Drug factory · FDA FEI 3014120699
Delpharm DIjon
6 boulevard de l'Europe, Quetigny, France
Problems found, fixed voluntarily at FDA's last inspection, Dec 13, 2024.
Voluntary Action Indicated: inspectors found problems, but not serious enough for FDA to take action. The company is expected to fix them.
2 drug inspections on record since 2021: 0 with no problems, 2 with problems fixed voluntarily, 0 with FDA action.
What it does, for whom
| Drug | Role | For | NDC |
|---|---|---|---|
| Pasireotide | Makes it | Recordati Rare Diseases, Inc. | 55292-131, 55292-132, 55292-133 |
FDA inspection history
| Ended | Result | Program | Problems noted |
|---|---|---|---|
| Dec 13, 2024 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| Nov 19, 2021 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
Registered with FDA for: manufacture; pack.