FDA inspection

Sunrise Distributors Inc: FDA inspection ending Jul 9, 2018

FDA inspection 1058311 · Voluntary Action Indicated (VAI) · Elk Grove Village, IL

Key facts

Inspection ID 1058311
Firm Sunrise Distributors Inc
FEI number 3009214777
Address 2411 United Ln
City Elk Grove Village
State IL
ZIP 60007
Country United States
Fiscal year 2018
Inspection end date Jul 9, 2018
Classification Voluntary Action Indicated (VAI)
Project area Foodborne Biological Hazards
Product type Food/Cosmetics

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes 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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