# Eprt Technologies Inc Dba Thrisoint – FDA Inspection, Apr 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 of Eprt Technologies Inc Dba Thrisoint, April 20, 2012. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. 1 other FDA inspection on record for this company.

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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)
- 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 941351 - 2015-09-09

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