# Trinity Biotech USA – FDA Inspection, May 4, 2012

Source: https://www.keypedia.com/records/fda_inspections/trinity-biotech-usa/86cbb93a-5a50-4224-8589-2a7b6fe51b48
Source feed: FDA_Inspections

> FDA inspection 780448 of Trinity Biotech USA, May 04, 2012. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 806 and 820. 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 780448
- Company Name: Trinity Biotech USA
- Inspection Date: 2012-05-04
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 1024021 - 2017-09-01](https://www.keypedia.com/records/fda_inspections/trinity-biotech-usa/f8350606-cca7-47e3-8bd6-678463ee3669)
- FDA Inspection 865821 - 2014-02-07

Company: https://www.keypedia.com/companies/trinity-biotech-usa/84422892-686f-47c7-a656-eab43686e40f

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7