# Veniti, Inc. – FDA Inspection, Jul 20, 2018

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

> FDA inspection 1059665 of Veniti, Inc., July 20, 2018. Classification: No Action Indicated (NAI). 1 citation under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 879437 - 2014-05-21

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/quynh-strandberg/9b582ae6-85f9-4163-8ce6-b179c5fd340e)

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

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