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FDA Inspection
•Abbvie Biotechnology Ltd.•October 30, 2023

Abbvie Biotechnology Ltd. – FDA Inspection, Oct 30, 2023

Record Details

This FDA Inspection record concerns Abbvie Biotechnology Ltd., with an inspection on October 30, 2023, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Abbvie Biotechnology Ltd.
Inspection Date
October 30, 2023
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Jose E. Melendez (FDA Associated Person)
View Company Profile

ID · fbc58704-0c5e-4f2c-8caa-a8e38cd2ba1a

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1222107
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Abbvie Biotechnology Ltd.

10
DateClassificationOfficeProject area
June 10, 2026Not classifiedSan Juan District OfficeDrug Quality Assurance
March 25, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 1, 2018VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 28, 2017VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 13, 2017Not classifiedSan Juan District Office
View all 10 other inspections on the company page
Other documents for Abbvie Biotechnology Ltd.
  • FDA Inspection 1321476 - 2026-06-10
  • FDA Inspection 1084057 - 2019-03-25
  • FDA Inspection 1055102 - 2018-06-01
  • FDA Inspection 1012249 - 2017-04-28
  • FDA Inspection 1001477 - 2017-01-13

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