FDA inspection

E.A. Beck & Co.: FDA inspection ending Aug 10, 2017

FDA inspection 1022942 · No Action Indicated (NAI) · Schaumburg, IL

Key facts

Inspection ID 1022942
Firm E.A. Beck & Co.
FEI number 2080222
Address 1507 W Alton Ave
City Schaumburg
State IL
ZIP 60173
Country United States
Fiscal year 2017
Inspection end date Aug 10, 2017
Classification No Action Indicated (NAI)
Project area Compliance: 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
  • 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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