# Viant Medical Company – FDA Inspection, Aug 22, 2018

Source: https://www.keypedia.com/records/fda_inspections/viant-medical-company/4a95b51a-682b-4199-a4b7-ac0a2568476d
Source feed: FDA_Inspections

> FDA inspection 1066023 of Viant Medical Company, August 22, 2018. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1066023
- Company Name: Viant Medical Company
- Inspection Date: 2018-08-22
- 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: 0

## Related Documents

- FDA Inspection 977051 - 2016-06-29
- [FDA Inspection 894949 - 2014-09-11](https://www.keypedia.com/records/fda_inspections/viant-medical-company/ea5b3e11-79fa-400f-94ca-59b26158f7eb)
- FDA Inspection 802129 - 2012-09-25
- FDA Inspection 702871 - 2010-12-15

## Related Officers

- [Sargum C. Morgan](https://www.keypedia.com/people/sargum-c-morgan/a769e36a-3382-414a-b9b1-1ebc755c8392)

Company: https://www.keypedia.com/companies/viant-medical-company/283687bb-6e5b-4b12-b030-fef9250c7162

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