Wasserburger Arzneimittelwerk GmbH
Wasserburger Arzneimittelwerk GmbH is a drug establishment in Wasserburg a Inn, Germany, registered with the US FDA under FEI 3002806849. Its registered operations are: Analytical testing, Labelling, Drug manufacture, Packaging. 24 EU/UK GMP certificates are matched to this site, 8 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 (24)
| Document | Authority | Inspection | Source |
|---|---|---|---|
DE_BY_04_GMP_2025_0036 GMP certificate | Competent authority of Germany | 13 Feb 2025 within 3-year review window | EudraGMDP |
DE_BY_04_GMP_2025_0035 GMP certificate | Competent authority of Germany | 13 Feb 2025 within 3-year review window | EudraGMDP |
DE_BY_04_GMP_2025_0185 GMP certificate | Competent authority of Germany | 13 Feb 2025 within 3-year review window | EudraGMDP |
DE_BY_04_GMP_2025_0034 GMP certificate | Competent authority of Germany | 13 Feb 2025 within 3-year review window | EudraGMDP |
DE_BY_04_GMP_2025_0183 GMP certificate | Competent authority of Germany | 13 Feb 2025 within 3-year review window | EudraGMDP |
DE_BY_04_GMP_2025_0186 GMP certificate | Competent authority of Germany | 13 Feb 2025 within 3-year review window | EudraGMDP |
DE_BY_04_GMP_2025_0184 GMP certificate | Competent authority of Germany | 13 Feb 2025 within 3-year review window | EudraGMDP |
DE_BY_04_GMP_2025_0037 GMP certificate | Competent authority of Germany | 13 Feb 2025 within 3-year review window | EudraGMDP |
DE_BY_04_GMP_2024_0100 GMP certificate | Competent authority of Germany | 30 Jun 2022 outside 3-year review window | EudraGMDP |
DE_BY_04_GMP_2024_0007 GMP certificate | Competent authority of Germany | 30 Jun 2022 outside 3-year review window | EudraGMDP |
DE_BY_04_GMP_2023_0146 GMP certificate | Competent authority of Germany | 30 Jun 2022 outside 3-year review window | EudraGMDP |
DE_BY_04_GMP_2024_0010 GMP certificate | Competent authority of Germany | 30 Jun 2022 outside 3-year review window | EudraGMDP |
DE_BY_04_GMP_2024_0022 GMP certificate | Competent authority of Germany | 30 Jun 2022 outside 3-year review window | EudraGMDP |
DE_BY_04_GMP_2024_0009 GMP certificate | Competent authority of Germany | 30 Jun 2022 outside 3-year review window | EudraGMDP |
DE_BY_04_GMP_2024_0101 GMP certificate | Competent authority of Germany | 30 Jun 2022 outside 3-year review window | EudraGMDP |
DE_BY_04_GMP_2023_0147 GMP certificate | Competent authority of Germany | 30 Jun 2022 outside 3-year review window | EudraGMDP |
DE_BY_04_GMP_2023_0143 GMP certificate | Competent authority of Germany | 30 Jun 2022 outside 3-year review window | EudraGMDP |
DE_BY_04_GMP_2023_0142 GMP certificate | Competent authority of Germany | 30 Jun 2022 outside 3-year review window | EudraGMDP |
DE_BY_04_GMP_2024_0020 GMP certificate | Competent authority of Germany | 30 Jun 2022 outside 3-year review window | EudraGMDP |
DE_BY_04_GMP_2024_0023 GMP certificate | Competent authority of Germany | 30 Jun 2022 outside 3-year review window | EudraGMDP |
DE_BY_04_GMP_2024_0008 GMP certificate | Competent authority of Germany | 30 Jun 2022 outside 3-year review window | EudraGMDP |
DE_BY_04_GMP_2024_0021 GMP certificate | Competent authority of Germany | 30 Jun 2022 outside 3-year review window | EudraGMDP |
DE_BY_04_GMP_2024_0103 GMP certificate | Competent authority of Germany | 30 Jun 2022 outside 3-year review window | EudraGMDP |
DE_BY_04_GMP_2024_0102 GMP certificate | Competent authority of Germany | 30 Jun 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.