# Vionic Group  LLC – FDA Inspection, Oct 12, 2016

Source: https://www.keypedia.com/records/fda_inspections/vionic-group-llc/89dbe6c7-e446-4f06-8c0a-029e96b40535
Source feed: FDA_Inspections

> FDA inspection 1003859 of Vionic Group  LLC, October 12, 2016. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1003859
- Company Name: Vionic Group  LLC
- Inspection Date: 2016-10-12
- 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 Officers

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

Company: https://www.keypedia.com/companies/vionic-group-llc/27367390-eb9b-4a10-bfb5-4d0890b4ae7c

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