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FDA Inspection
•AbbVie Inc.•December 15, 2017

AbbVie Inc. – FDA Inspection, Dec 15, 2017

Record Details

This FDA Inspection record concerns AbbVie Inc., with an inspection on December 15, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
AbbVie Inc.
Inspection Date
December 15, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Debra I. Love (FDA Associated Person)
  • Michele Perry-Williams (FDA Associated Person)
  • Robert J. Ham (FDA Associated Person)
  • Tenzin Jangchup (FDA Associated Person)
View Company Profile

ID · 84aefdfd-48f8-4eeb-99a2-dea21a624924

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1037506
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of AbbVie Inc.

21
DateClassificationOfficeProject area
April 27, 2026Not classifiedChicago District Office
April 2, 2026Not classifiedChicago District Office
August 21, 2025Not classifiedChicago District Office
June 12, 2025NAICenter for Biologics Evaluation and ResearchBioresearch Monitoring
February 18, 2025Not classifiedChicago District Office
View all 21 other inspections on the company page
Other documents for AbbVie Inc.
  • FDA Inspection 1299008 - 2026-04-27
  • FDA Inspection 1302298 - 2026-04-02
  • FDA Inspection 1277010 - 2025-08-21
  • FDA Inspection 1257605 - 2025-06-12
  • FDA Inspection 1230795 - 2025-02-18

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