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Kaneka Eurogentec SA — FDA Facility Profile

FEI 3003323169

Kaneka Eurogentec SA is an FDA-registered facility (FEI 3003323169) located in Liege B-4102, BE. Registered operations: ANALYSIS; API MANUFACTURE. RegDataLab tracks 6 FDA inspections at this facility.

Facility Details

Location
Liege B-4102 (BE)
Registration Expires
December 31, 2026
Operations
ANALYSIS; API MANUFACTURE
Source
decrs

Recent inspections

  • 1323182 (VAI Mon Feb 26 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1205117 (VAI Tue Apr 06 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1037724 (VAI Fri Oct 27 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 907804 (VAI Fri Dec 19 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 835985 (VAI Thu Mar 28 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 756607 (VAI Thu Oct 27 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Import refusals

  • SCS-2012451-9/11/1 (Mon Nov 23 2020 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)

FDA data resources