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FDA Inspection 870006 — Morton Grove Pharmaceuticals, Inc.

Morton Grove Pharmaceuticals, Inc. — FEI 1420913

The FDA completed an inspection of Morton Grove Pharmaceuticals, Inc. on March 26, 2014 in Morton Grove, IL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 26, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Morton Grove, IL (United States)

Facility

Other inspections at this facility

  • 964577 (OAI Fri Feb 05 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 702633 (VAI Tue Apr 12 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 651880 (VAI Wed Mar 24 2010 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 614298 (NAI Thu Sep 17 2009 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 568902 (VAI Tue Mar 17 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources