# FDA Inspection 783154 - Eprt Technologies Inc Dba Thrisoint - April 20, 2012

Source: https://www.keypedia.com/records/fda_inspections/eprt-technologies-inc-dba-thrisoint/b3c65b0b-7093-49c0-b2bb-25d3670cc362
Source feed: FDA_Inspections

> FDA Inspection 783154 for Eprt Technologies Inc Dba Thrisoint on April 20, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 783154
- Company Name: Eprt Technologies Inc Dba Thrisoint
- Inspection Date: 2012-04-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 941351 - 2015-09-09](https://www.keypedia.com/records/fda_inspections/eprt-technologies-inc-dba-thrisoint/4d417e95-11c8-4c76-b731-9c5264ed3561)

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