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FDA Inspection
•Curium Netherlands B.V.•June 13, 2024

Curium Netherlands B.V. – FDA Inspection, Jun 13, 2024

Record Details

This FDA Inspection record concerns Curium Netherlands B.V., with an inspection on June 13, 2024, issued by the Center for Devices and Radiological Health, covering devices.

Company
Curium Netherlands B.V.
Inspection Date
June 13, 2024
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Christopher W. Buser (Issuing Officer)
View Company Profile

ID · 0343b087-e460-4ce9-a1d0-2c9384bda003

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1243632
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Curium Netherlands B.V.

5
DateClassificationOfficeProject area
May 17, 2024Not classifiedOffice of Inspections and Investigations
January 16, 2020VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 1, 2018VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 18, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 1, 2011NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Curium Netherlands B.V.
  • FDA Inspection 1320892 - 2024-05-17
  • FDA Inspection 1129626 - 2020-01-16
  • FDA Inspection 1056705 - 2018-06-01
  • FDA Inspection 956581 - 2015-12-18
  • FDA Inspection 739038 - 2011-07-01

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