FDA inspection

Morton Grove Pharmaceuticals, Inc.: FDA inspection ending Jan 9, 2008

FDA inspection 504795 · No Action Indicated (NAI) · Morton Grove, IL

Key facts

Inspection ID 504795
Firm Morton Grove Pharmaceuticals, Inc.
FEI number 1420913
Address 6451 Main St
City Morton Grove
State IL
ZIP 60053-2633
Fiscal year 2008
Inspection end date Jan 9, 2008
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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