FDA inspection

Sunrise Distributors Inc: FDA inspection ending Dec 5, 2019

FDA inspection 1111862 · Official Action Indicated (OAI) · Elk Grove Village, IL

Key facts

Inspection ID 1111862
Firm Sunrise Distributors Inc
FEI number 3009214777
Address 2411 United Ln
City Elk Grove Village
State IL
ZIP 60007
Country United States
Fiscal year 2020
Inspection end date Dec 5, 2019
Classification Official Action Indicated (OAI)
Project area Foodborne Biological Hazards
Product type Food/Cosmetics
Warning letter 599020

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • Yes 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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