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FDA Inspection
•Primus Corporation dba Trinity Biotech•September 17, 2021

Primus Corporation dba Trinity Biotech – FDA Inspection, Sep 17, 2021

Record Details

This FDA Inspection record concerns Primus Corporation dba Trinity Biotech, with an inspection on September 17, 2021, issued by the Center for Devices and Radiological Health, covering devices.

Company
Primus Corporation dba Trinity Biotech
Inspection Date
September 17, 2021
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · d88c3399-8472-41e6-bc2f-1d05cc243eef

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1154252
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

Other FDA inspections of Primus Corporation dba Trinity Biotech

7
DateClassificationOfficeProject area
September 26, 2022NAICenter for Devices and Radiological HealthCompliance: Devices
February 6, 2020OAICenter for Devices and Radiological HealthCompliance: Devices
September 5, 2019Not classifiedKansas City District Office
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 1117396 - 2020-02-06
  • FDA Inspection 1122890 - 2019-09-05
  • FDA Inspection 1064644 - 2018-09-06
  • FDA Inspection 912071 - 2015-01-30

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