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FDA Inspection
•Curium US, LLC•March 27, 2013

Curium US, LLC – FDA Inspection, Mar 27, 2013

Record Details

This FDA Inspection record concerns Curium US, LLC, with an inspection on March 27, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company
Curium US, LLC
Inspection Date
March 27, 2013
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · e452fa95-d533-4a3a-a7c9-5a862cdba9d9

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
828678
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Curium US, LLC

10
DateClassificationOfficeProject area
September 18, 2024NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
August 18, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 18, 2018NAICenter for Devices and Radiological HealthCompliance: Devices
November 18, 2016Not classifiedKansas City District Office
November 13, 2015NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
View all 10 other inspections on the company page
Other documents for Curium US, LLC
  • FDA Inspection 1250722 - 2024-09-18
  • FDA Inspection 1216202 - 2023-08-18
  • FDA Inspection 1080170 - 2018-12-18
  • FDA Inspection 996388 - 2016-11-18
  • FDA Inspection 966441 - 2015-11-13

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