FDA Inspection
Curium Netherlands B.V.Curium Netherlands B.V. – FDA Inspection, Jun 1, 2018
Record Details
This FDA Inspection record concerns Curium Netherlands B.V., with an inspection on June 1, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · f6284b7e-80c2-4591-b5aa-65fbbb66497a
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1056705
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Curium Netherlands B.V.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| June 13, 2024 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 17, 2024 | Not classified | Office of Inspections and Investigations | |
| January 16, 2020 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| December 18, 2015 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 1, 2011 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Curium Netherlands B.V.
- FDA Inspection 1243632 - 2024-06-13
- FDA Inspection 1320892 - 2024-05-17
- FDA Inspection 1129626 - 2020-01-16
- FDA Inspection 956581 - 2015-12-18
- FDA Inspection 739038 - 2011-07-01
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