Medifix, Inc.

Form 483

Morton Grove, Illinois, United StatesFEI 3003444211Issued October 15, 2009

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 3003444211.

Observations1

Issue DateOctober 15, 2009

StatusNo Warning Letter

Related Inspections3

Establishment Details

Firm: Medifix, Inc.
Location: Morton Grove, Illinois, United States
FEI Number: 3003444211
Product Type: Devices
Issue Date: October 15, 2009
Country: United States

Inspection History, 2009 to 2017

NAI1

VAI2

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

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Medifix, Inc. FDA Form 483, Morton Grove, Illinois, October 15, 2009