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FDA Inspection
•Abbott Medical•August 2, 2019

Abbott Medical – FDA Inspection, Aug 2, 2019

Record Details

This FDA Inspection record concerns Abbott Medical, with an inspection on August 2, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company
Abbott Medical
Inspection Date
August 2, 2019
Product Type
Devices
Office
Center for Devices and Radiological Health
People
  • Leonard H. Lavi (FDA Associated Person)
  • Nicole M Gillette (Issuing Officer)
View Company Profile

ID · e91fc62f-e5fd-4e40-bf99-2045d51618b8

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1099418
FDA center
Medical Devices & Rad Health
Project area
Bioresearch Monitoring
Outcome
Form 483 issued

Other FDA inspections of Abbott Medical

13
DateClassificationOfficeProject area
June 28, 2023VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
January 17, 2020NAICenter for Devices and Radiological HealthBioresearch Monitoring
September 20, 2018Not classifiedLos Angeles District Office
February 17, 2017OAICenter for Devices and Radiological HealthCompliance: Devices
March 24, 2016NAICenter for Devices and Radiological HealthCompliance: Devices
View all 13 other inspections on the company page
Other documents for Abbott Medical
  • FDA Inspection 1209394 - 2023-06-28
  • FDA Inspection 1120476 - 2020-01-17
  • FDA Inspection 1122945 - 2018-09-20
  • FDA Inspection 1000696 - 2017-02-17
  • FDA Inspection 964165 - 2016-03-24

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