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FDA Inspection
•TriMed Inc.•June 3, 2024

TriMed Inc. – FDA Inspection, Jun 3, 2024

Record Details

This FDA Inspection record concerns TriMed Inc., with an inspection on June 3, 2024, issued by the Los Angeles District Office, covering medical devices & rad health.

Company
TriMed Inc.
Inspection Date
June 3, 2024
Product Type
Medical Devices & Rad Health
Office
Los Angeles District Office
Person
  • Kelvin Cheung (Issuing Officer)
View Company Profile

ID · 90b20c29-6681-4bf3-a153-2d5d28dbfa71

Inspection Facts

Inspection number
1240179
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices
Outcome
Form 483 issued

FDA Citations

2
  1. 21 CFR 820.100(b)Documentation
  2. 21 CFR 820.30(f)Design verification - documentation

Full citation text and observation details available on the Dashboard.

Other FDA inspections of TriMed Inc.

5
DateClassificationOfficeProject area
August 14, 2019NAICenter for Devices and Radiological HealthPostmarket Assurance: 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 1103478 - 2019-08-14
  • 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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