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FDA Inspection
•Amgen, Inc.•June 17, 2013

Amgen, Inc. – FDA Inspection, Jun 17, 2013

Record Details

This FDA Inspection record concerns Amgen, Inc., with an inspection on June 17, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company
Amgen, Inc.
Inspection Date
June 17, 2013
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · c575b5cf-dc57-44f7-b4dc-6b4703b35f94

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
837193
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Amgen, Inc.

29
DateClassificationOfficeProject area
August 7, 2025Not classifiedLos Angeles District Office
March 13, 2025VAILos Angeles District OfficeDrug Quality Assurance
February 6, 2024Not classifiedLos Angeles District Office
September 14, 2023NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
December 13, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 29 other inspections on the company page
Other documents for Amgen, Inc.
  • FDA Inspection 1278976 - 2025-08-07
  • FDA Inspection 1256132 - 2025-03-13
  • FDA Inspection 1240449 - 2024-02-06
  • FDA Inspection 1220409 - 2023-09-14
  • FDA Inspection 1112791 - 2019-12-13

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