# FDA Inspection 1013967 - Trevi Technology Inc - June 06, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/trevi-technology-inc/735fac58-4f82-4883-8c0b-0b9566b30597
Source feed: FDA_Inspections

> FDA Inspection 1013967 for Trevi Technology Inc on June 06, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1013967
- Company Name: Trevi Technology Inc
- Inspection Date: 2017-06-06
- 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 1072317 - 2018-11-06](https://www.globalkeysolutions.net/records/fda_inspections/trevi-technology-inc/8f387485-7526-491f-887d-1cb755d0bc8e)
- [FDA Inspection 1072317 - 2018-11-06](https://www.globalkeysolutions.net/records/fda_inspections/trevi-technology-inc/3d8b8bee-fa8c-4a9d-a682-46a02ed71c9c)
- [FDA Inspection 1013967 - 2017-06-06](https://www.globalkeysolutions.net/records/fda_inspections/trevi-technology-inc/44f95887-ca98-40a9-8563-783ca824daf9)

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

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