FDA Inspection
Amgen, Inc.Amgen, Inc. – FDA Inspection, Feb 17, 2017
Record Details
This FDA Inspection record concerns Amgen, Inc., with an inspection on February 17, 2017, issued by the Los Angeles District Office, covering human drugs.
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ID · dfcbfff9-f283-46a3-8a41-7fb8f7b5f014
Inspection Facts
- Inspection number
- 1015989
- FDA center
- Human Drugs
- Outcome
- Form 483 issued
Other FDA inspections of Amgen, Inc.
29| Date | Classification | Office | Project area |
|---|---|---|---|
| August 7, 2025 | Not classified | Los Angeles District Office | |
| March 13, 2025 | VAI | Los Angeles District Office | Drug Quality Assurance |
| February 6, 2024 | Not classified | Los Angeles District Office | |
| September 14, 2023 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| December 13, 2019 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
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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