Medtronic Perfusion Systems

Form 483

Brooklyn Park, Minnesota, United StatesFEI 1000116158Issued September 30, 2016

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 1000116158.

Observations4

Issue DateSeptember 30, 2016

StatusNo Warning Letter

Related Inspections8

Establishment Details

Firm: Medtronic Perfusion Systems
Location: Brooklyn Park, Minnesota, United States
FEI Number: 1000116158
Product Type: Devices
Issue Date: September 30, 2016
Country: United States

Inspection History, 2009 to 2022

NAI7

VAI1

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

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Medtronic Perfusion Systems FDA Form 483, Brooklyn Park, Minnesota, September 30, 2016