Medtronic MiniMed, Inc.

Form 483

Northridge, California, United StatesFEI 3003166194Issued July 22, 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 3003166194.

Observations1

Issue DateJuly 22, 2016

StatusNo Warning Letter

Related Inspections10

Establishment Details

Firm: Medtronic MiniMed, Inc.
Location: Northridge, California, United States
FEI Number: 3003166194
Product Type: Devices
Issue Date: July 22, 2016
Country: United States

Inspection History, 2014 to 2024

NAI4

VAI5

OAI1

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

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Medtronic MiniMed, Inc. FDA Form 483, Northridge, California, July 22, 2016