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483
•Allergan Pharmaceuticals Ireland•January 30, 2025

Allergan Pharmaceuticals Ireland – FDA 483, Jan 30, 2025

Record Details

Allergan Pharmaceuticals Ireland Unlimited, a drug product manufacturer in Westport, Ireland, was cited for multiple deficiencies during an FDA inspection. The observations included inadequate visual inspection rejection limits, insufficient laboratory test procedures for endotoxin, and a lack of cleaning validation for indirect product contact parts. Further issues were noted in environmental monitoring for aseptic processing areas and shipping validation for samples.

Company
Allergan Pharmaceuticals Ireland
Inspection date
January 30, 2025
Product type
drugs
Office
Office of Inspections and Investigations
People
  • Jie He
  • Thuy T. Nguyen ( Investigator, Consumer Safety Officer)
  • Kejun Cheng (other)
View Company Profile

ID · 621f52b2-bbcb-409b-ab8f-70a89c613fd3

Other documents for Allergan Pharmaceuticals Ireland
  • 483 - 2019-12-17December 17, 2019

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