Fresenius Kabi Austria

Austria 8055, AustriaFEI 3003708554

Fresenius Kabi Austria is a drug establishment in Austria 8055, Austria, registered with the US FDA under FEI 3003708554. Its registered operations are: Analytical testing, Drug manufacture, Packaging, Repackaging. 24 EU/UK GMP certificates are matched to this site, 19 inspected within the last three years.

Sources: FDA Drug Establishments Current Registration Site (checked 2 Nov 2026); EudraGMDP; MHRA GMDP. Methodology

Registered operations

Business operations this establishment declares in its FDA registration. Registration is not an approval and says nothing about EU or UK GMP status.

Analytical testingDrug manufacturePackagingRepackaging

GMP documents matched to this site (24)

DocumentAuthorityInspectionSource
480166-104335423
GMP certificate
Competent authority of Austria18 Jul 2025
within 3-year review window
EudraGMDP
480166-105403093
GMP certificate
Competent authority of Austria18 Jul 2025
within 3-year review window
EudraGMDP
480166-104835425
GMP certificate
Competent authority of Austria18 Jul 2025
within 3-year review window
EudraGMDP
480166-104999511
GMP certificate
Competent authority of Austria18 Jul 2025
within 3-year review window
EudraGMDP
480166-105121500
GMP certificate
Competent authority of Austria18 Jul 2025
within 3-year review window
EudraGMDP
480166-104693690
GMP certificate
Competent authority of Austria18 Jul 2025
within 3-year review window
EudraGMDP
480166-103608964
GMP certificate
Competent authority of Austria18 Jul 2025
within 3-year review window
EudraGMDP
482159-105717637
GMP certificate
Competent authority of Austria7 Nov 2024
within 3-year review window
EudraGMDP
482159-102663721
GMP certificate
Competent authority of Austria7 Nov 2024
within 3-year review window
EudraGMDP
482159-105567534
GMP certificate
Competent authority of Austria7 Nov 2024
within 3-year review window
EudraGMDP
482159-104397091
GMP certificate
Competent authority of Austria7 Nov 2024
within 3-year review window
EudraGMDP
482159-104999541
GMP certificate
Competent authority of Austria7 Nov 2024
within 3-year review window
EudraGMDP
480166-102491361
GMP certificate
Competent authority of Austria21 Mar 2024
within 3-year review window
EudraGMDP
480166-102607179
GMP certificate
Competent authority of Austria21 Mar 2024
within 3-year review window
EudraGMDP
480166-102423596
GMP certificate
Competent authority of Austria21 Mar 2024
within 3-year review window
EudraGMDP
480166-102774477
GMP certificate
Competent authority of Austria21 Mar 2024
within 3-year review window
EudraGMDP
480166-101575058
GMP certificate
Competent authority of Austria28 Nov 2023
within 3-year review window
EudraGMDP
480166-101688176
GMP certificate
Competent authority of Austria28 Nov 2023
within 3-year review window
EudraGMDP
480166-102295520
GMP certificate
Competent authority of Austria28 Nov 2023
within 3-year review window
EudraGMDP
482159-102378631
GMP certificate
Competent authority of Austria13 Oct 2022
outside 3-year review window
EudraGMDP
482159-102091741
GMP certificate
Competent authority of Austria13 Oct 2022
outside 3-year review window
EudraGMDP
482159-103505366
GMP certificate
Competent authority of Austria13 Oct 2022
outside 3-year review window
EudraGMDP
480166-102091568
GMP certificate
Competent authority of Austria14 Jan 2022
outside 3-year review window
EudraGMDP
480166-102298815
GMP certificate
Competent authority of Austria14 Jan 2022
outside 3-year review window
EudraGMDP

A GMP document is matched to this site when its address names the site's street and its city or postcode. In our latest internal review 59 of 60 sampled matches were the right site (not yet independently reviewed; measured match quality). Check the certificate's own address before relying on it. The three-year review window is the EMA guideline default after an inspection, not an official expiry date.

What this page does not show

  • Which substances are made here: DMFs and CEPs are filed by organisations, not sites, so we do not link substances to this site.
  • Capacity, scale, price or current availability: no regulator publishes these.
  • FDA inspection classifications for this site, which are not yet linked.

Other sites registered by the same company