Medtronic Neuromodulation

Form 483

Minneapolis, Minnesota, United StatesFEI 2182207Issued June 30, 2017

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 2182207.

Observations2

Issue DateJune 30, 2017

StatusNo Warning Letter

Related Inspections10

Establishment Details

Firm: Medtronic Neuromodulation
Location: Minneapolis, Minnesota, United States
FEI Number: 2182207
Product Type: Devices
Issue Date: June 30, 2017
Country: United States

Inspection History, 2013 to 2023

NAI3

VAI7

NAI means No Action Indicated. VAI means Voluntary Action Indicated.

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Medtronic Neuromodulation FDA Form 483, Minneapolis, Minnesota, June 30, 2017