# FDA Inspection 1059665 - Veniti, Inc. - July 20, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/veniti-inc/e1797d7a-ac1f-4c23-9593-e24cfc485938
Source feed: FDA_Inspections

> FDA Inspection 1059665 for Veniti, Inc. on July 20, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1059665
- Company Name: Veniti, Inc.
- Inspection Date: 2018-07-20
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 879437 - 2014-05-21](https://www.globalkeysolutions.net/records/fda_inspections/veniti-inc/06931a3c-3a2e-431a-b8ce-4572eb6b43d2)
- [FDA Inspection 879437 - 2014-05-21](https://www.globalkeysolutions.net/records/fda_inspections/veniti-inc/06223b8f-653e-4d0a-82c4-a37042e5985d)

Company: https://www.globalkeysolutions.net/companies/veniti-inc/827e815d-c01e-473a-b8d6-38529b1b47d3

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