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.
Observations3
Issue DateMarch 18, 2013
StatusNo Warning Letter
Related Inspections3
Establishment Details
Firm
Medifix, Inc.
Location
Morton Grove, Illinois, United States
FEI Number
3003444211
Product Type
Devices
Issue Date
March 18, 2013
Country
United States
Inspection History, 2009 to 2017
NAI1
VAI2
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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