# Trevi Technology Inc – FDA Inspection, Nov 6, 2018

Source: https://www.keypedia.com/records/fda_inspections/trevi-technology-inc/8f387485-7526-491f-887d-1cb755d0bc8e
Source feed: FDA_Inspections

> FDA inspection 1072317 of Trevi Technology Inc, November 06, 2018. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1072317
- Company Name: Trevi Technology Inc
- Inspection Date: 2018-11-06
- 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: 3

## Related Documents

- [FDA Inspection 1013967 - 2017-06-06](https://www.keypedia.com/records/fda_inspections/trevi-technology-inc/735fac58-4f82-4883-8c0b-0b9566b30597)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/javonica-f-penn/56294265-08fc-4d1d-8a34-626fc4dad457)

Company: https://www.keypedia.com/companies/trevi-technology-inc/f33d7882-ad49-4fd8-8ef5-275328a9a003

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