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FDA Inspection
•Amgen, Inc.•May 16, 2017

Amgen, Inc. – FDA Inspection, May 16, 2017

Record Details

This FDA Inspection record concerns Amgen, Inc., with an inspection on May 16, 2017, issued by the Los Angeles District Office, covering human drugs.

Company
Amgen, Inc.
Inspection Date
May 16, 2017
Product Type
Human Drugs
Office
Los Angeles District Office
Person
  • Laura Fontan (Company Rep)
View Company Profile

ID · 418eba20-ce54-43d8-8579-bc1c6529fdc5

Inspection Facts

Inspection number
1017093
FDA center
Human Drugs
Outcome
Form 483 issued

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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