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FDA Inspection 1108882 — Fareva Morton Grove, Inc.

Fareva Morton Grove, Inc. — FEI 1410794

The FDA completed an inspection of Fareva Morton Grove, Inc. on September 18, 2019 in Morton Grove, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 18, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Morton Grove, IL (United States)

Facility

Other inspections at this facility

  • 1278907 (OAI Tue Aug 12 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 960749 (NAI Tue Feb 02 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 772922 (NAI Mon Mar 19 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 635207 (NAI Fri Nov 06 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources