FDA Inspection 1020990 - Orthoaccel Technologies, Inc - February 17, 2017

FDA Inspection 1020990 for Orthoaccel Technologies, Inc on February 17, 2017. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1020990 for Orthoaccel Technologies, Inc on February 17, 2017. Classification: No Action Indicated (NAI).

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Record Information

Company

Orthoaccel Technologies, Inc

Inspection Date

February 17, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: ffd9dbda-fec1-4fec-bf6c-a9dae1a2f612

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