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FDA Inspection
•AVID Medical, Inc.•May 24, 2024

AVID Medical, Inc. – FDA Inspection, May 24, 2024

Record Details

This FDA Inspection record concerns AVID Medical, Inc., with an inspection on May 24, 2024, issued by the Center for Devices and Radiological Health, covering devices.

Company
AVID Medical, Inc.
Inspection Date
May 24, 2024
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Heath A. Gerber (Investigator)
View Company Profile

ID · db4c1c75-d134-4d65-bce3-f481c42baccd

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1240582
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

Other FDA inspections of AVID Medical, Inc.

6
DateClassificationOfficeProject area
December 5, 2022VAICenter for Devices and Radiological HealthCompliance: Devices
August 5, 2021NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
April 5, 2019NAICenter for Devices and Radiological HealthCompliance: Devices
April 4, 2016NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
December 19, 2013NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
View all 6 other inspections on the company page
Other documents for AVID Medical, Inc.
  • FDA Inspection 1192303 - 2022-12-05
  • FDA Inspection 1156265 - 2021-08-05
  • FDA Inspection 1090400 - 2019-04-05
  • FDA Inspection 968475 - 2016-04-04
  • FDA Inspection 861014 - 2013-12-19

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