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FDA Inspection
•TriMed Inc.•August 14, 2019

TriMed Inc. – FDA Inspection, Aug 14, 2019

Record Details

This FDA Inspection record concerns TriMed Inc., with an inspection on August 14, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company
TriMed Inc.
Inspection Date
August 14, 2019
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Kelvin Cheung (Issuing Officer)
View Company Profile

ID · 9f150df8-927c-43f6-b716-0c54bbda2b97

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1103478
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

Other FDA inspections of TriMed Inc.

5
DateClassificationOfficeProject area
June 3, 2024Not classifiedLos Angeles District OfficeCompliance: Devices
November 17, 2017VAICenter for Devices and Radiological HealthCompliance: Devices
January 12, 2017VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
March 18, 2016OAICenter for Devices and Radiological HealthCompliance: Devices
January 25, 2012VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for TriMed Inc.
  • FDA Inspection 1240179 - 2024-06-03
  • FDA Inspection 1031588 - 2017-11-17
  • FDA Inspection 998813 - 2017-01-12
  • FDA Inspection 963328 - 2016-03-18
  • FDA Inspection 766423 - 2012-01-25

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