FDA Inspection 993576 - Perseon Corporation - November 30, 2016

FDA Inspection 993576 for Perseon Corporation on November 30, 2016. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 993576 for Perseon Corporation on November 30, 2016. Classification: No Action Indicated (NAI).

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Record Information

Company

Perseon Corporation

Inspection Date

November 30, 2016

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 1d74eaab-39b2-4c22-b02a-1eb8205800c9

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