FDA Inspection 1002313 - CardioRenal Systems, Inc. - February 28, 2017

FDA Inspection 1002313 for CardioRenal Systems, Inc. on February 28, 2017. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1002313 for CardioRenal Systems, Inc. on February 28, 2017. Classification: No Action Indicated (NAI).

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Record Information

Company

CardioRenal Systems, Inc.

Inspection Date

February 28, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fba08884-d142-4ce2-a9e3-d1cad7f61829

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