FDA Inspection 992735 - Medtronic CryoCath LP - October 27, 2016

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Record Details

This FDA Inspection record concerns Medtronic CryoCath LP, with an inspection on October 27, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: Medtronic CryoCath LP
Inspection Date: October 27, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 784c201c-b1f4-4843-bfc6-f3a921408d8e