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FDA Inspection
•Allergan Pharmaceuticals Ireland•January 30, 2025

Allergan Pharmaceuticals Ireland – FDA Inspection, Jan 30, 2025

Record Details

This FDA Inspection record concerns Allergan Pharmaceuticals Ireland, with an inspection on January 30, 2025, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Allergan Pharmaceuticals Ireland
Inspection Date
January 30, 2025
Product Type
Human Drugs
Office
Office of Inspections and Investigations
People
  • Jie He (Issuing Officer)
  • Thuy T. Nguyen (FDA Associated Person)
View Company Profile

ID · 5cd0cdac-a1ee-429c-bf97-7a8c1777a54a

Inspection Facts

Inspection number
1259046
FDA center
Human Drugs
Outcome
Form 483 issued, view the record

Other FDA inspections of Allergan Pharmaceuticals Ireland

8
DateClassificationOfficeProject area
June 17, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 4, 2018VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 16, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 3, 2015VAICenter for Devices and Radiological HealthCompliance: Devices
July 11, 2013NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 8 other inspections on the company page
Other documents for Allergan Pharmaceuticals Ireland
  • FDA Inspection 1194596 - 2022-06-17
  • FDA Inspection 1117366 - 2018-05-04
  • FDA Inspection 1002463 - 2016-12-16
  • FDA Inspection 933338 - 2015-07-03
  • FDA Inspection 842267 - 2013-07-11

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