FDA Inspection 960560 - Axiobionics, LLC - February 18, 2016

FDA Inspection 960560 for Axiobionics, LLC on February 18, 2016. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 960560 for Axiobionics, LLC on February 18, 2016. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Axiobionics, LLC

Inspection Date

February 18, 2016

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 6655a236-f2b1-45bb-9365-c765a654d97e

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