Excella GmbH & Co. KG

Feucht, GermanyFEI 3000242652API manufacture registered

Excella GmbH & Co. KG is a drug establishment in Feucht, Germany, registered with the US FDA under FEI 3000242652. Its registered operations are: Analytical testing, API manufacture, Labelling, Drug manufacture, Packaging. 40 EU/UK GMP certificates are matched to this site, 37 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 manufactureLabellingDrug manufacturePackaging

GMP documents matched to this site (40)

DocumentAuthorityInspectionSource
DE_BY_05_GMP_2026_0144
GMP certificate
Competent authority of Germany24 Apr 2026
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0097
GMP certificate
Competent authority of Germany24 Apr 2026
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0096
GMP certificate
Competent authority of Germany24 Apr 2026
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0095
GMP certificate
Competent authority of Germany24 Apr 2026
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0145
GMP certificate
Competent authority of Germany24 Apr 2026
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0127
GMP certificate
Competent authority of Germany24 Mar 2026
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0139
GMP certificate
Competent authority of Germany24 Mar 2026
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0087
GMP certificate
Competent authority of Germany24 Mar 2026
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0140
GMP certificate
Competent authority of Germany24 Mar 2026
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0135
GMP certificate
Competent authority of Germany24 Mar 2026
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0113
GMP certificate
Competent authority of Germany24 Mar 2026
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0092
GMP certificate
Competent authority of Germany24 Mar 2026
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0137
GMP certificate
Competent authority of Germany24 Mar 2026
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0088
GMP certificate
Competent authority of Germany24 Mar 2026
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0138
GMP certificate
Competent authority of Germany24 Mar 2026
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0141
GMP certificate
Competent authority of Germany24 Mar 2026
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0143
GMP certificate
Competent authority of Germany24 Mar 2026
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0136
GMP certificate
Competent authority of Germany24 Mar 2026
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0112
GMP certificate
Competent authority of Germany24 Mar 2026
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0090
GMP certificate
Competent authority of Germany24 Mar 2026
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0076
GMP certificate
Competent authority of Germany24 Mar 2026
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0091
GMP certificate
Competent authority of Germany24 Mar 2026
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0075
GMP certificate
Competent authority of Germany24 Mar 2026
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0086
GMP certificate
Competent authority of Germany24 Mar 2026
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0077
GMP certificate
Competent authority of Germany24 Mar 2026
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0129
GMP certificate
EU competent authority24 Mar 2026
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0089
GMP certificate
Competent authority of Germany24 Mar 2026
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0083
GMP certificate
Competent authority of Germany24 Mar 2026
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0133
GMP certificate
Competent authority of Germany24 Mar 2026
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0134
GMP certificate
Competent authority of Germany24 Mar 2026
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0142
GMP certificate
Competent authority of Germany24 Mar 2026
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0046
GMP certificate
Competent authority of Germany25 Jul 2025
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0008
GMP certificate
Competent authority of Germany25 Jul 2025
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0012
GMP certificate
Competent authority of Germany25 Jul 2025
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0013
GMP certificate
Competent authority of Germany25 Jul 2025
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0047
GMP certificate
Competent authority of Germany25 Jul 2025
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2026_0009
GMP certificate
Competent authority of Germany25 Jul 2025
within 3-year review window
EudraGMDP
DE_BY_05_GMP_2023_0054
GMP certificate
Competent authority of Germany15 Sept 2023
outside 3-year review window
EudraGMDP
DE_BY_05_GMP_2023_0053
GMP certificate
Competent authority of Germany15 Sept 2023
outside 3-year review window
EudraGMDP
DE_BY_05_GMP_2023_0055
GMP certificate
Competent authority of Germany15 Sept 2023
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.