Boehringer Ingelheim RCV GmbH & Co KG

Vienna, AustriaFEI 3003433722API manufacture registered

Boehringer Ingelheim RCV GmbH & Co KG is a drug establishment in Vienna, Austria, registered with the US FDA under FEI 3003433722. Its registered operations are: Analytical testing, API manufacture. 30 EU/UK GMP certificates are matched to this site, 16 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 testingAPI manufacture

GMP documents matched to this site (30)

DocumentAuthorityInspectionSource
480011-104799526
GMP certificate
Competent authority of Austria11 Jun 2026
within 3-year review window
EudraGMDP
480011-105183503
GMP certificate
Competent authority of Austria4 Jul 2025
within 3-year review window
EudraGMDP
480011-103599005
GMP certificate
Competent authority of Austria4 Jul 2025
within 3-year review window
EudraGMDP
480011-102584426
GMP certificate
Competent authority of Austria20 Feb 2024
within 3-year review window
EudraGMDP
480011-103399880
GMP certificate
Competent authority of Austria20 Feb 2024
within 3-year review window
EudraGMDP
480011-103641677
GMP certificate
Competent authority of Austria20 Feb 2024
within 3-year review window
EudraGMDP
480011-102831158
GMP certificate
Competent authority of Austria20 Feb 2024
within 3-year review window
EudraGMDP
480011-103252488
GMP certificate
Competent authority of Austria20 Feb 2024
within 3-year review window
EudraGMDP
480011-104203702
GMP certificate
Competent authority of Austria20 Feb 2024
within 3-year review window
EudraGMDP
480011-103843386
GMP certificate
Competent authority of Austria20 Feb 2024
within 3-year review window
EudraGMDP
480011-102624876
GMP certificate
Competent authority of Austria16 Feb 2024
within 3-year review window
EudraGMDP
480011-102614673
GMP certificate
Competent authority of Austria16 Feb 2024
within 3-year review window
EudraGMDP
480011-102625178
GMP certificate
Competent authority of Austria16 Feb 2024
within 3-year review window
EudraGMDP
480011-102633078
GMP certificate
Competent authority of Austria16 Feb 2024
within 3-year review window
EudraGMDP
480011-102625209
GMP certificate
Competent authority of Austria16 Feb 2024
within 3-year review window
EudraGMDP
480011-102275025
GMP certificate
Competent authority of Austria15 Feb 2024
within 3-year review window
EudraGMDP
480011-102027428
GMP certificate
Competent authority of Austria2 Mar 2023
outside 3-year review window
EudraGMDP
480011-101924884
GMP certificate
Competent authority of Austria2 Mar 2023
outside 3-year review window
EudraGMDP
480011-101618405
GMP certificate
Competent authority of Austria2 Mar 2023
outside 3-year review window
EudraGMDP
480011-102338375
GMP certificate
Competent authority of Austria2 Mar 2023
outside 3-year review window
EudraGMDP
480011-101925737
GMP certificate
Competent authority of Austria2 Mar 2023
outside 3-year review window
EudraGMDP
480011-102387067
GMP certificate
Competent authority of Austria2 Mar 2023
outside 3-year review window
EudraGMDP
480011-102174974
GMP certificate
Competent authority of Austria2 Mar 2023
outside 3-year review window
EudraGMDP
480011-100896010
GMP certificate
Competent authority of Austria2 Mar 2023
outside 3-year review window
EudraGMDP
480011-101128884
GMP certificate
Competent authority of Austria16 Sept 2021
outside 3-year review window
EudraGMDP
480011-13975060
GMP certificate
Competent authority of Austria16 Sept 2021
outside 3-year review window
EudraGMDP
480011-101202174
GMP certificate
Competent authority of Austria16 Sept 2021
outside 3-year review window
EudraGMDP
480011-101042130
GMP certificate
Competent authority of Austria16 Sept 2021
outside 3-year review window
EudraGMDP
480011-101366736
GMP certificate
Competent authority of Austria16 Sept 2021
outside 3-year review window
EudraGMDP
480011-101424874
GMP certificate
Competent authority of Austria16 Sept 2021
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.