FDA inspection

U.S. Durum Milling, Inc.: FDA inspection ending May 14, 2019

FDA inspection 1094455 · No Action Indicated (NAI) · Saint Louis, MO

Key facts

Inspection ID 1094455
Firm U.S. Durum Milling, Inc.
FEI number 1938005
Address 7900 Van Buren St
City Saint Louis
State MO
ZIP 63111
Country United States
Fiscal year 2019
Inspection end date May 14, 2019
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
  • 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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