Baxter Deutschland GmbH

Bielefeld, GermanyFEI 3002806414API manufacture registered

Baxter Deutschland GmbH is a drug establishment in Bielefeld, Germany, registered with the US FDA under FEI 3002806414. Its registered operations are: API manufacture. 3 EU/UK GMP certificates are matched to this site, 1 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.

API manufacture

GMP documents matched to this site (3)

DocumentAuthorityInspectionSource
DE_NW_02_GMP_2025_0014
GMP certificate
Competent authority of Germany28 May 2025
within 3-year review window
EudraGMDP
DE_NW_02_GMP_2023_0019
GMP certificate
Competent authority of Germany8 Apr 2022
outside 3-year review window
EudraGMDP
DE_NW_02_GMP_2023_0016
GMP certificate
Competent authority of Germany8 Apr 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