# FDA Inspection 1024021 - Trinity Biotech USA - September 01, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/trinity-biotech-usa/e90c161c-d5ba-4901-86b8-84e80da25aca
Source feed: FDA_Inspections

> FDA Inspection 1024021 for Trinity Biotech USA on September 01, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1024021
- Company Name: Trinity Biotech USA
- Inspection Date: 2017-09-01
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1024021 - 2017-09-01](https://www.globalkeysolutions.net/records/fda_inspections/trinity-biotech-usa/f8350606-cca7-47e3-8bd6-678463ee3669)
- [FDA Inspection 865821 - 2014-02-07](https://www.globalkeysolutions.net/records/fda_inspections/trinity-biotech-usa/1a149fec-7866-41b1-9bf2-3e17923b4ac2)
- [FDA Inspection 865821 - 2014-02-07](https://www.globalkeysolutions.net/records/fda_inspections/trinity-biotech-usa/2ef42755-3d1d-47c7-bbe0-ef8b0838f766)
- [FDA Inspection 865821 - 2014-02-07](https://www.globalkeysolutions.net/records/fda_inspections/trinity-biotech-usa/bbb6d654-e421-4ffb-b600-14fba6e48702)
- [FDA Inspection 780448 - 2012-05-04](https://www.globalkeysolutions.net/records/fda_inspections/trinity-biotech-usa/2cc8f528-2b44-4efe-bc1e-ce5f8ef71ed5)

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

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