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FDA Inspection
•GE Healthcare Inc.•March 8, 2024

GE Healthcare Inc. – FDA Inspection, Mar 8, 2024

Record Details

This FDA Inspection record concerns GE Healthcare Inc., with an inspection on March 8, 2024, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
GE Healthcare Inc.
Inspection Date
March 8, 2024
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Kent A. Conforti (Company Rep)
  • Meredith L. Miller
View Company Profile

ID · ab3eaa59-c633-46ea-8be0-e091bbd9031c

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1232232
FDA center
Human Drugs
Project area
Bioresearch Monitoring

FDA Citations

1
  1. 21 CFR 312.50Ensuring compliance with plan and protocol

Full citation text and observation details available on the Dashboard.

Other FDA inspections of GE Healthcare Inc.

9
DateClassificationOfficeProject area
September 19, 2025NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
October 2, 2023Not classifiedChicago District Office
January 24, 2020NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 6, 2017NAICenter for Devices and Radiological HealthCompliance: Devices
March 5, 2015NAICenter for Devices and Radiological HealthCompliance: Devices
View all 9 other inspections on the company page
Other documents for GE Healthcare Inc.
  • FDA Inspection 1287530 - 2025-09-19
  • FDA Inspection 1221712 - 2023-10-02
  • FDA Inspection 1117219 - 2020-01-24
  • FDA Inspection 1026911 - 2017-09-06
  • FDA Inspection 916324 - 2015-03-05

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