FDA Inspection 1014720 - Venus Concept Inc - May 02, 2017

FDA Inspection 1014720 for Venus Concept Inc on May 02, 2017. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1014720 for Venus Concept Inc on May 02, 2017. Classification: No Action Indicated (NAI).

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Record Information

Company

Venus Concept Inc

Inspection Date

May 2, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 291d3941-1619-42a9-a429-39480a439c15

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