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FDA Inspection
•Abbott Laboratories GmbH•February 24, 2017

Abbott Laboratories GmbH – FDA Inspection, Feb 24, 2017

Record Details

This FDA Inspection record concerns Abbott Laboratories GmbH, with an inspection on February 24, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Abbott Laboratories GmbH
Inspection Date
February 24, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Lucila B. Nwatu (FDA Associated Person)
View Company Profile

ID · 32c87f90-f0b1-41a2-9580-a85ead30b8cc

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1017658
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Abbott Laboratories GmbH

6
DateClassificationOfficeProject area
May 30, 2024VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 30, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
October 24, 2014NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 19, 2013NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 11, 2010NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 6 other inspections on the company page
Other documents for Abbott Laboratories GmbH
  • FDA Inspection 1274874 - 2024-05-30
  • FDA Inspection 1107966 - 2019-08-30
  • FDA Inspection 904481 - 2014-10-24
  • FDA Inspection 830369 - 2013-04-19
  • FDA Inspection 682154 - 2010-06-11

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