Home / Inspections / 746885

FDA Inspection 746885 — Medefil Incorporated

Medefil Incorporated — FEI 3001677091

The FDA completed an inspection of Medefil Incorporated on September 6, 2011 in Glendale Heights, IL. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
September 6, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Glendale Heights, IL (United States)

Facility

Other inspections at this facility

  • 1251304 (VAI Mon Apr 21 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1046065 (VAI Thu Mar 29 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 976257 (VAI Fri Jun 17 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 894968 (VAI Mon Sep 15 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 808935 (VAI Thu Dec 20 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources