FDA Inspection 1253044 - Medtronic CryoCath LP - October 31, 2024

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Record Details

This FDA Inspection record concerns Medtronic CryoCath LP, with an inspection on October 31, 2024, issued by the Center for Devices and Radiological Health, covering devices.

Company: Medtronic CryoCath LP
Inspection Date: October 31, 2024
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · a9bdba1d-ebc0-4936-8e58-3df10ff326f5

Violation Codes1

21 CFR 820.86

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