# FDA Inspection 1003859 - Vionic Group  LLC - October 12, 2016

Source: https://www.keypedia.com/records/fda_inspections/vionic-group-llc/18f8fa7a-3690-4c04-98e2-6ebc1f720305
Source feed: FDA_Inspections

> FDA Inspection 1003859 for Vionic Group  LLC on October 12, 2016. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1003859
- Company Name: Vionic Group  LLC
- Inspection Date: 2016-10-12
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1003859 - 2016-10-12](https://www.keypedia.com/records/fda_inspections/vionic-group-llc/89dbe6c7-e446-4f06-8c0a-029e96b40535)

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