Drug factory · FDA FEI 3017440477
AqVida GmbH
Werkstr. 21, Dassow, Germany
Problems found, fixed voluntarily at FDA's last inspection, Dec 5, 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 2022: 0 with no problems, 2 with problems fixed voluntarily, 0 with FDA action.
What it does, for whom
| Drug | Role | For | NDC |
|---|---|---|---|
| Nelarabine | Makes it | Shorla Oncology Inc. | 81927-111, 81927-375 |
FDA inspection history
| Ended | Result | Program | Problems noted |
|---|---|---|---|
| Dec 5, 2024 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| Dec 8, 2022 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
Registered with FDA for: analysis; label; manufacture; pack.