FDA inspection

GEXPRO, a Division of REXEL USA Inc: FDA inspection ending Sep 23, 2024

FDA inspection 1252511 · No Action Indicated (NAI) · Menomonee Falls, WI

Key facts

Inspection ID 1252511
Firm GEXPRO, a Division of REXEL USA Inc
FEI number 3007545404
Address W134n5450 Campbell Dr
City Menomonee Falls
State WI
ZIP 53051
Country United States
Fiscal year 2024
Inspection end date Sep 23, 2024
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

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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