CU Chemie Uetikon GmbH

Lahr, GermanyFEI 3002806757API manufacture registered

CU Chemie Uetikon GmbH is a drug establishment in Lahr, Germany, registered with the US FDA under FEI 3002806757. Its registered operations are: Analytical testing, API manufacture. 12 EU/UK GMP certificates are matched to this site, 12 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 (12)

DocumentAuthorityInspectionSource
DE_BW_01_GMP_2025_0106
GMP certificate
Competent authority of Germany30 Jan 2025
within 3-year review window
EudraGMDP
DE_BW_01_GMP_2025_0110
GMP certificate
Competent authority of Germany30 Jan 2025
within 3-year review window
EudraGMDP
DE_BW_01_GMP_2025_0105
GMP certificate
Competent authority of Germany30 Jan 2025
within 3-year review window
EudraGMDP
DE_BW_01_GMP_2025_0108
GMP certificate
Competent authority of Germany30 Jan 2025
within 3-year review window
EudraGMDP
DE_BW_01_GMP_2025_0109
GMP certificate
Competent authority of Germany30 Jan 2025
within 3-year review window
EudraGMDP
DE_BW_01_GMP_2025_0102
GMP certificate
Competent authority of Germany30 Jan 2025
within 3-year review window
EudraGMDP
DE_BW_01_GMP_2025_0103
GMP certificate
Competent authority of Germany30 Jan 2025
within 3-year review window
EudraGMDP
DE_BW_01_GMP_2025_0104
GMP certificate
Competent authority of Germany30 Jan 2025
within 3-year review window
EudraGMDP
DE_BW_01_GMP_2025_0107
GMP certificate
Competent authority of Germany30 Jan 2025
within 3-year review window
EudraGMDP
DE_BW_01_GMP_2025_0100
GMP certificate
Competent authority of Germany30 Jan 2025
within 3-year review window
EudraGMDP
DE_BW_01_GMP_2026_0165
GMP certificate
Competent authority of Germany30 Jan 2025
within 3-year review window
EudraGMDP
DE_BW_01_GMP_2025_0101
GMP certificate
Competent authority of Germany30 Jan 2025
within 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.