Source: FDA record for this establishment. FDA publishes inspections or enforcement actions for this establishment, listed further down this page, but we have not matched this particular Form 483 to a document or an inspection date FDA has released. It stays out of the default view for that reason. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3001677091.
Observations6
Issue DateFebruary 19, 2009
StatusNo Warning Letter
Related Inspections10
Establishment Details
Firm
Medefil Incorporated
Location
Glendale Heights, Illinois, United States
FEI Number
3001677091
Product Type
Devices
Issue Date
February 19, 2009
Country
United States
Inspection History, 2010 to 2025
NAI2
VAI6
OAI2
NAI means No Action Indicated. VAI means Voluntary Action Indicated. OAI means Official Action Indicated.