# Trinity Biotech USA – FDA Inspection, Sep 1, 2017

Source: https://www.keypedia.com/records/fda_inspections/trinity-biotech-usa/f8350606-cca7-47e3-8bd6-678463ee3669
Source feed: FDA_Inspections

> FDA inspection 1024021 of Trinity Biotech USA, September 01, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1024021
- Company Name: Trinity Biotech USA
- Inspection Date: 2017-09-01
- 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: 1

## Related Documents

- FDA Inspection 865821 - 2014-02-07
- [FDA Inspection 780448 - 2012-05-04](https://www.keypedia.com/records/fda_inspections/trinity-biotech-usa/86cbb93a-5a50-4224-8589-2a7b6fe51b48)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/matthew-d-schnittker/cf76f07f-db6d-47a0-8412-7eb084d4fe8b)

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