Excella GmbH & Co. KG
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.
GMP documents matched to this site (40)
| Document | Authority | Inspection | Source |
|---|---|---|---|
DE_BY_05_GMP_2026_0144 GMP certificate | Competent authority of Germany | 24 Apr 2026 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0097 GMP certificate | Competent authority of Germany | 24 Apr 2026 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0096 GMP certificate | Competent authority of Germany | 24 Apr 2026 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0095 GMP certificate | Competent authority of Germany | 24 Apr 2026 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0145 GMP certificate | Competent authority of Germany | 24 Apr 2026 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0127 GMP certificate | Competent authority of Germany | 24 Mar 2026 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0139 GMP certificate | Competent authority of Germany | 24 Mar 2026 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0087 GMP certificate | Competent authority of Germany | 24 Mar 2026 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0140 GMP certificate | Competent authority of Germany | 24 Mar 2026 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0135 GMP certificate | Competent authority of Germany | 24 Mar 2026 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0113 GMP certificate | Competent authority of Germany | 24 Mar 2026 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0092 GMP certificate | Competent authority of Germany | 24 Mar 2026 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0137 GMP certificate | Competent authority of Germany | 24 Mar 2026 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0088 GMP certificate | Competent authority of Germany | 24 Mar 2026 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0138 GMP certificate | Competent authority of Germany | 24 Mar 2026 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0141 GMP certificate | Competent authority of Germany | 24 Mar 2026 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0143 GMP certificate | Competent authority of Germany | 24 Mar 2026 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0136 GMP certificate | Competent authority of Germany | 24 Mar 2026 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0112 GMP certificate | Competent authority of Germany | 24 Mar 2026 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0090 GMP certificate | Competent authority of Germany | 24 Mar 2026 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0076 GMP certificate | Competent authority of Germany | 24 Mar 2026 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0091 GMP certificate | Competent authority of Germany | 24 Mar 2026 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0075 GMP certificate | Competent authority of Germany | 24 Mar 2026 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0086 GMP certificate | Competent authority of Germany | 24 Mar 2026 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0077 GMP certificate | Competent authority of Germany | 24 Mar 2026 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0129 GMP certificate | EU competent authority | 24 Mar 2026 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0089 GMP certificate | Competent authority of Germany | 24 Mar 2026 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0083 GMP certificate | Competent authority of Germany | 24 Mar 2026 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0133 GMP certificate | Competent authority of Germany | 24 Mar 2026 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0134 GMP certificate | Competent authority of Germany | 24 Mar 2026 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0142 GMP certificate | Competent authority of Germany | 24 Mar 2026 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0046 GMP certificate | Competent authority of Germany | 25 Jul 2025 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0008 GMP certificate | Competent authority of Germany | 25 Jul 2025 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0012 GMP certificate | Competent authority of Germany | 25 Jul 2025 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0013 GMP certificate | Competent authority of Germany | 25 Jul 2025 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0047 GMP certificate | Competent authority of Germany | 25 Jul 2025 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2026_0009 GMP certificate | Competent authority of Germany | 25 Jul 2025 within 3-year review window | EudraGMDP |
DE_BY_05_GMP_2023_0054 GMP certificate | Competent authority of Germany | 15 Sept 2023 outside 3-year review window | EudraGMDP |
DE_BY_05_GMP_2023_0053 GMP certificate | Competent authority of Germany | 15 Sept 2023 outside 3-year review window | EudraGMDP |
DE_BY_05_GMP_2023_0055 GMP certificate | Competent authority of Germany | 15 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.