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483
•Amgen Manufacturing Ltd•February 27, 2020

Amgen Manufacturing Ltd – FDA 483, Feb 27, 2020

Record Details

An FDA inspection of Amgen Manufacturing, Limited (AML) in Juncos, PR, revealed significant deficiencies in quality control systems for drug substance manufacturing. The firm failed to adequately investigate critical utility and environmental monitoring excursions, and lacked assurance that critical equipment remained in a validated state. Additionally, there were issues with the qualification of clean utilities and the effectiveness of cleaning procedures for product-contact equipment.

Company
Amgen Manufacturing Ltd
Inspection date
February 27, 2020
Product type
drugs
Office
Division of Clinical Evidence and Analysis 1 (Clinical Policy and Quality)
People
  • Wendy G. Tan
  • Zhong Li
View Company Profile

ID · abc3f33a-b3af-41e0-a0aa-af0692b345ae

Other documents for Amgen Manufacturing Ltd
  • 483 - 2023-07-05July 5, 2023
  • 483 - 2021-09-08September 8, 2021
  • EIR - 2019-09-27September 27, 2019
  • 483 - 2019-09-27September 27, 2019
  • 483 - 2019-05-08May 8, 2019

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