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

FDA Inspection 960560 for Axiobionics, LLC on February 18, 2016. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 960560 for Axiobionics, LLC on February 18, 2016. Classification: No Action Indicated (NAI).

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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: 3e317ea8-4081-472e-860b-7ac23e02c4fd

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