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FDA Inspection 639896 — Medefil Incorporated

Medefil Incorporated — FEI 3001677091

The FDA completed an inspection of Medefil Incorporated on February 11, 2010 in Glendale Heights, IL. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
February 11, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Glendale Heights, IL (United States)

Facility

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Recent compliance actions

FDA data resources