FDA inspection

GEXPRO, a Division of REXEL USA Inc: FDA inspection ending Aug 26, 2011

FDA inspection 742200 · No Action Indicated (NAI) · Menomonee Falls, WI

Key facts

Inspection ID 742200
Firm GEXPRO, a Division of REXEL USA Inc
FEI number 3007545404
Address 12221 W Feerick St
City Menomonee Falls
State WI
ZIP 53051
Country United States
Fiscal year 2011
Inspection end date Aug 26, 2011
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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