FDA Inspection 985385 - Michael Snyder MD - June 09, 2016

FDA Inspection 985385 for Michael Snyder MD on June 09, 2016. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 985385 for Michael Snyder MD on June 09, 2016. Classification: No Action Indicated (NAI).

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Record Information

Company

Michael Snyder MD

Inspection Date

June 9, 2016

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fd44f029-f77e-445f-a969-83b4887ba50f

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