Home / Inspections / 742200

FDA Inspection 742200 — GEXPRO, a Division of REXEL USA Inc

GEXPRO, a Division of REXEL USA Inc — FEI 3007545404

The FDA completed an inspection of GEXPRO, a Division of REXEL USA Inc on August 26, 2011 in Menomonee Falls, WI. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 26, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Menomonee Falls, WI (United States)

Facility

Other inspections at this facility

  • 1252511 (NAI Mon Sep 23 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1120075 (NAI Fri Feb 14 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 949230 (NAI Fri Sep 25 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 684651 (VAI Tue Oct 12 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources