GE Inspection Technologies, LP

FDA Regulatory Profile

GE Inspection Technologies, LP appears in FDA public data with 8 recalls, 0 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent recall (Z-0442-2021, Class II) was initiated on September 29, 2020.

Summary

Total Recalls
8
510(k) Clearances
0
Inspections
1
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-0442-2021Class IIv|tome|x L Series non-destructive testing cabinet x-ray systemsSeptember 29, 2020
Z-2777-2017Class IIGE Inspection Technologies Blade|line Industrial Cabinet X-ray systemJune 28, 2017
Z-2236-2016Class IIGE Inspection Technologies, LP - Phoenix v|tome|x m240 cabinet x-ray systems. A microfocus CT sysMarch 2, 2016
Z-1231-2016Class IIGE Inspection Technologies, LP, Cabinet X-ray system used for industrial quality control.December 16, 2015
Z-1225-2015Class IIGE Inspection Technologies x|argos 160D system. Cabinet x-ray system.January 13, 2015
Z-1211-2015Class IIGE Inspection Technologies x|tome|x L240 an Cabinet X-ray systemJanuary 13, 2015
Z-0426-2015Class IIGE Cabinet X-ray systemsNovember 10, 2014
Z-2320-2015Class IIGE Optional Laser Centering Device X-ray generator.November 10, 2014