FDA Inspection 976895 - Medtronic Perfusion Systems - June 17, 2016

FDA Inspection 976895 for Medtronic Perfusion Systems on June 17, 2016. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 976895 for Medtronic Perfusion Systems on June 17, 2016. Classification: No Action Indicated (NAI).

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Record Information

Company

Medtronic Perfusion Systems

Inspection Date

June 17, 2016

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f65aacdc-c341-4fbf-88e1-238a0b868a34

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