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FDA Inspection
•Primus Corporation dba Trinity Biotech•January 30, 2015

Primus Corporation dba Trinity Biotech – FDA Inspection, Jan 30, 2015

Record Details

This FDA Inspection record concerns Primus Corporation dba Trinity Biotech, with an inspection on January 30, 2015, issued by the Center for Devices and Radiological Health, covering devices.

Company
Primus Corporation dba Trinity Biotech
Inspection Date
January 30, 2015
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 9cf309a4-2bce-4777-94eb-3c13ba9c32bc

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
912071
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
September 17, 2021NAICenter for Devices and Radiological HealthPostmarket Assurance: 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
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 1122890 - 2019-09-05
  • FDA Inspection 1064644 - 2018-09-06

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