FDA inspection

EDLONG CORPORATION: FDA inspection ending Nov 28, 2018

FDA inspection 1074031 · No Action Indicated (NAI) · Elk Grove Village, IL

Key facts

Inspection ID 1074031
Firm EDLONG CORPORATION
FEI number 1413301
Address 225 Scott St
City Elk Grove Village
State IL
ZIP 60007
Country United States
Fiscal year 2019
Inspection end date Nov 28, 2018
Classification No Action Indicated (NAI)
Project area Foodborne Biological Hazards
Product type Food/Cosmetics

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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