# Bionix, Llc – FDA Inspection, Jul 14, 2026

Source: https://www.keypedia.com/records/fda_inspections/bionix-llc/e6874ab6-4d74-4e0e-b4f2-94cf12046a80
Source feed: FDA_Inspections

> FDA inspection 1326218 of Bionix, Llc, July 14, 2026. Classification: Voluntary Action Indicated (VAI). 8 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: 1326218
- Company Name: Bionix, Llc
- Inspection Date: 2026-07-14
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Cincinnati District Office
- Citation Count: 8

## Related Documents

- [FDA Inspection 1179655 - 2022-09-02](https://www.keypedia.com/records/fda_inspections/bionix-llc/a2f9949c-993f-4cad-af75-a09ecd84cfdb)
- [FDA Inspection 1024053 - 2017-08-24](https://www.keypedia.com/records/fda_inspections/bionix-llc/653d5ed7-5895-4bce-b1e6-e04e8e659b17)
- [FDA Inspection 979145 - 2016-06-23](https://www.keypedia.com/records/fda_inspections/bionix-llc/e0e16ab3-105d-4259-8b62-aa4179e89414)
- [FDA Inspection 854680 - 2013-11-21](https://www.keypedia.com/records/fda_inspections/bionix-llc/ce510154-d8d1-4057-af50-f866b85ae49a)
- [FDA Inspection 667265 - 2010-06-17](https://www.keypedia.com/records/fda_inspections/bionix-llc/faa1ebf4-fd61-4631-aa83-f289f6f8e485)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/felicia-e-armbrustmacher/83e0f3f7-2bfc-4250-8627-76685eee6b03)

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

Office: https://www.keypedia.com/offices/cincinnati-district-office/b67a0c35-82e3-4176-9039-988378f65c22