FDA Inspection 979214 - Medtronic MiniMed, Inc. - July 22, 2016

FDA Inspection 979214 for Medtronic MiniMed, Inc. on July 22, 2016. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 979214 for Medtronic MiniMed, Inc. on July 22, 2016. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 812.140(b)(2)

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Record Information

Company

Medtronic MiniMed, Inc.

Inspection Date

July 22, 2016

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fa028779-d558-4c57-a043-35d5441d57b9

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