# FDA Inspection 941351 - Eprt Technologies Inc Dba Thrisoint - September 09, 2015

Source: https://www.keypedia.com/records/fda_inspections/eprt-technologies-inc-dba-thrisoint/4d417e95-11c8-4c76-b731-9c5264ed3561
Source feed: FDA_Inspections

> FDA Inspection 941351 for Eprt Technologies Inc Dba Thrisoint on September 09, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 941351
- Company Name: Eprt Technologies Inc Dba Thrisoint
- Inspection Date: 2015-09-09
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 783154 - 2012-04-20](https://www.keypedia.com/records/fda_inspections/eprt-technologies-inc-dba-thrisoint/b3c65b0b-7093-49c0-b2bb-25d3670cc362)

Company: https://www.keypedia.com/companies/eprt-technologies-inc-dba-thrisoint/469dcc68-0266-4935-b000-1fb3f71fc846

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