# Bionix, Llc – FDA Inspection, Aug 24, 2017

Source: https://www.keypedia.com/records/fda_inspections/bionix-llc/653d5ed7-5895-4bce-b1e6-e04e8e659b17
Source feed: FDA_Inspections

> FDA inspection 1024053 of Bionix, Llc, August 24, 2017. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR part 820. Form 483 issued. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1024053
- Company Name: Bionix, Llc
- Inspection Date: 2017-08-24
- 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: 5

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## Related Officers

- [Company Rep](https://www.keypedia.com/people/javonica-f-penn/56294265-08fc-4d1d-8a34-626fc4dad457)

Company: https://www.keypedia.com/companies/bionix-llc/19876df5-bcee-496c-985f-38115caf87ed

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