# Venni Instruments Inc – FDA Inspection, Jan 17, 2018

Source: https://www.keypedia.com/records/fda_inspections/venni-instruments-inc/fe680c97-4eec-4692-909e-0321507460e9
Source feed: FDA_Inspections

> FDA inspection 1038015 of Venni Instruments Inc, January 17, 2018. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1038015
- Company Name: Venni Instruments Inc
- Inspection Date: 2018-01-17
- 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: 1

## Related Documents

- FDA Inspection 920978 - 2015-03-31
- [FDA Inspection 810371 - 2012-12-13](https://www.keypedia.com/records/fda_inspections/venni-instruments-inc/86760eca-09aa-4b8c-ab90-16ef3195c9be)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/ronald-ifraimov/b4ce8b79-3fa2-4862-b7a4-68e14e45d87a)

Company: https://www.keypedia.com/companies/venni-instruments-inc/ec6009bf-be86-4e20-afc2-e37d95191d1e

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