FDA Inspection 982335 - Nevro Corporation - August 26, 2016

FDA Inspection 982335 for Nevro Corporation on August 26, 2016. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 982335 for Nevro Corporation on August 26, 2016. Classification: No Action Indicated (NAI).

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Record Information

Company

Nevro Corporation

Inspection Date

August 26, 2016

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fbf655b9-857c-4367-bd7c-daa9638322e1

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