Fresenius Kabi Deutschland GmbH
Fresenius Kabi Deutschland GmbH is a drug establishment in Friedberg, Germany, registered with the US FDA under FEI 3002851530. Its registered operations are: Analytical testing, Drug manufacture. 8 EU/UK GMP certificates are matched to this site, 5 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 (8)
| Document | Authority | Inspection | Source |
|---|---|---|---|
DE_HE_01_GMP_2026_0057 GMP certificate | Competent authority of Germany | 5 Sept 2025 within 3-year review window | EudraGMDP |
DE_HE_01_GMP_2026_0038 GMP certificate | Competent authority of Germany | 5 Sept 2025 within 3-year review window | EudraGMDP |
DE_HE_01_GMP_2025_0246 GMP certificate | Competent authority of Germany | 15 Nov 2024 within 3-year review window | EudraGMDP |
DE_HE_01_GMP_2024_0264 GMP certificate | Competent authority of Germany | 21 Dec 2023 within 3-year review window | EudraGMDP |
DE_HE_01_GMP_2025_0039 GMP certificate | Competent authority of Germany | 21 Dec 2023 within 3-year review window | EudraGMDP |
DE_HE_01_GMP_2023_0159 GMP certificate | Competent authority of Germany | 19 Oct 2022 outside 3-year review window | EudraGMDP |
DE_HE_01_GMP_2024_0012 GMP certificate | Competent authority of Germany | 19 Oct 2022 outside 3-year review window | EudraGMDP |
DE_HE_01_GMP_2024_0076 GMP certificate | Competent authority of Germany | 5 Nov 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.