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FDA Inspection
•Primus Corporation dba Trinity Biotech•September 5, 2019

Primus Corporation dba Trinity Biotech – FDA Inspection, Sep 5, 2019

Record Details

This FDA Inspection record concerns Primus Corporation dba Trinity Biotech, with an inspection on September 5, 2019, issued by the Kansas City District Office, covering medical devices & rad health.

Company
Primus Corporation dba Trinity Biotech
Inspection Date
September 5, 2019
Product Type
Medical Devices & Rad Health
Office
Kansas City District Office
View Company Profile

ID · 5e8d2462-9976-4c7f-88fd-b26e43fb02b7

Inspection Facts

Inspection number
1122890
FDA center
Medical Devices & Rad Health
Outcome
Form 483 issued

Other FDA inspections of Primus Corporation dba Trinity Biotech

7
DateClassificationOfficeProject area
September 26, 2022NAICenter for Devices and Radiological HealthCompliance: Devices
September 17, 2021NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
February 6, 2020OAICenter for Devices and Radiological HealthCompliance: Devices
September 6, 2018OAICenter for Devices and Radiological HealthCompliance: Devices
January 30, 2015NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
View all 7 other inspections on the company page
Other documents for Primus Corporation dba Trinity Biotech
  • FDA Inspection 1180790 - 2022-09-26
  • FDA Inspection 1154252 - 2021-09-17
  • FDA Inspection 1117396 - 2020-02-06
  • FDA Inspection 1064644 - 2018-09-06
  • FDA Inspection 912071 - 2015-01-30

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