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FDA Inspection
•Medtronic CryoCath LP•October 27, 2016

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

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