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FDA Inspection
•Gibson Laboratories, LLC•April 29, 2010

Gibson Laboratories, LLC – FDA Inspection, Apr 29, 2010

Record Details

This FDA Inspection record concerns Gibson Laboratories, LLC, with an inspection on April 29, 2010, issued by the Center for Devices and Radiological Health, covering devices.

Company
Gibson Laboratories, LLC
Inspection Date
April 29, 2010
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · dee0d5d0-221c-4cca-afe6-0214ff5ea88a

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
659193
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Gibson Laboratories, LLC

5
DateClassificationOfficeProject area
April 25, 2024NAICenter for Devices and Radiological HealthCompliance: Devices
March 3, 2022NAICenter for Devices and Radiological HealthCompliance: Devices
November 2, 2017NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
December 12, 2013VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
September 14, 2009OAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Gibson Laboratories, LLC
  • FDA Inspection 1238338 - 2024-04-25
  • FDA Inspection 1165243 - 2022-03-03
  • FDA Inspection 1035086 - 2017-11-02
  • FDA Inspection 859677 - 2013-12-12
  • FDA Inspection 610286 - 2009-09-14

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