FDA Inspection 633459 - Medtronic CryoCath LP - December 10, 2009

FDA Inspection 633459 for Medtronic CryoCath LP on December 10, 2009. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 633459 for Medtronic CryoCath LP on December 10, 2009. Classification: No Action Indicated (NAI).

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Record Information

Company

Medtronic CryoCath LP

Inspection Date

December 10, 2009

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f6a42874-eb4c-4e81-8229-d047672adf12

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