FDA Inspection 1102180 - Medtronic Neuromodulation - August 06, 2019

FDA Inspection 1102180 for Medtronic Neuromodulation on August 06, 2019. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1102180 for Medtronic Neuromodulation on August 06, 2019. Classification: No Action Indicated (NAI).

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Record Information

Company

Medtronic Neuromodulation

Inspection Date

August 6, 2019

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: ffaaee90-31c0-4a0a-8024-c623571f25d7

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