FDA inspection

Fareva Morton Grove, Inc.: FDA inspection ending Sep 18, 2019

FDA inspection 1108882 · No Action Indicated (NAI) · Morton Grove, IL

Key facts

Inspection ID 1108882
Firm Fareva Morton Grove, Inc.
FEI number 1410794
Address 6901 Golf Rd
City Morton Grove
State IL
ZIP 60053
Country United States
Fiscal year 2019
Inspection end date Sep 18, 2019
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
  • No Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 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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