FDA Inspection 1005666 - Medtronic MiniMed, Inc. - March 24, 2017

FDA Inspection 1005666 for Medtronic MiniMed, Inc. on March 24, 2017. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1005666 for Medtronic MiniMed, Inc. on March 24, 2017. Classification: No Action Indicated (NAI).

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Record Information

Company

Medtronic MiniMed, Inc.

Inspection Date

March 24, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fa6d117d-ca0a-4b8c-af3e-742354fb7592

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