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FDA Inspection
•GE Healthcare AS•November 10, 2017

GE Healthcare AS – FDA Inspection, Nov 10, 2017

Record Details

This FDA Inspection record concerns GE Healthcare AS, with an inspection on November 10, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
GE Healthcare AS
Inspection Date
November 10, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Samantha J. Bradley (FDA Associated Person)
View Company Profile

ID · 765e0953-5fd7-4162-b821-5abb6cc37fef

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1037481
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of GE Healthcare AS

7
DateClassificationOfficeProject area
April 23, 2024VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 27, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 12, 2016NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 3, 2015NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 13, 2012VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 7 other inspections on the company page
Other documents for GE Healthcare AS
  • FDA Inspection 1236691 - 2024-04-23
  • FDA Inspection 1100537 - 2019-08-27
  • FDA Inspection 959608 - 2016-02-12
  • FDA Inspection 915526 - 2015-02-03
  • FDA Inspection 810910 - 2012-12-13

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