FDA Inspection 1052017 - Medtronic Inc. - May 14, 2018

FDA Inspection 1052017 for Medtronic Inc. on May 14, 2018. Classification: Official Action Indicated (OAI).

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Record Summary

FDA Inspection 1052017 for Medtronic Inc. on May 14, 2018. Classification: Official Action Indicated (OAI).

Violation Codes

21 CFR 820.100(a)

21 CFR 820.30(h)

21 CFR 820.70(b)

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Record Information

Company

Medtronic Inc.

Inspection Date

May 14, 2018

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fdca1d91-dbf2-4fae-95b0-2488ae45b8ff

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