FDA inspection

Keefe Group, LLC: FDA inspection ending Mar 29, 2024

FDA inspection 1236725 · No Action Indicated (NAI) · Saint Louis, MO

Key facts

Inspection ID 1236725
Firm Keefe Group, LLC
FEI number 3005452251
Address 10880 Linpage Pl
City Saint Louis
State MO
ZIP 63132
Country United States
Fiscal year 2024
Inspection end date Mar 29, 2024
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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