# Avant Wellness Systems, Inc. – FDA Inspection, Nov 8, 2017

Source: https://www.keypedia.com/records/fda_inspections/avant-wellness-systems-inc/f46469b7-90c8-4636-8c80-db90ae26977e
Source feed: FDA_Inspections

> FDA inspection 1031068 of Avant Wellness Systems, Inc., November 08, 2017. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR parts 803 and 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1031068
- Company Name: Avant Wellness Systems, Inc.
- Inspection Date: 2017-11-08
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

## Related Documents

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- FDA Inspection 1147628 - 2021-07-21

## Related Officers

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

Company: https://www.keypedia.com/companies/avant-wellness-systems-inc/1730624e-b410-4805-93a6-c59a7641e758

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