FDA inspection

Abbott Molecular, Inc.: FDA inspection ending Feb 19, 2021

FDA inspection 1136769 · No Action Indicated (NAI) · Des Plaines, IL

Key facts

Inspection ID 1136769
Firm Abbott Molecular, Inc.
FEI number 3005248192
Address 1300 E Touhy Ave
City Des Plaines
State IL
ZIP 60018
Country United States
Fiscal year 2021
Inspection end date Feb 19, 2021
Classification No Action Indicated (NAI)
Project area Project Evaluation: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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