FDA inspection

Lafarge Midwest, Inc: FDA inspection ending Sep 20, 2001

FDA inspection 88530 · No Action Indicated (NAI) · Saint Joseph, MI

Key facts

Inspection ID 88530
Firm Lafarge Midwest, Inc
FEI number 1829873
Address 200 Upton Dr
City Saint Joseph
State MI
ZIP 49085-1148
Fiscal year 2001
Inspection end date Sep 20, 2001
Classification No Action Indicated (NAI)
Project area Tech Assist: Food & Cosmetics
Product type Food/Cosmetics

At a glance

  • None Citations
  • None 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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