Intervet International GMBH

85716 Unterscheissheim, GermanyFEI 3003517550

Intervet International GMBH is a drug establishment in 85716 Unterscheissheim, Germany, registered with the US FDA under FEI 3003517550. Its registered operations are: Analytical testing, Labelling, Drug manufacture, Packaging, Relabelling, Repackaging, Sterilisation. 6 EU/UK GMP certificates are matched to this site, 3 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 testingLabellingDrug manufacturePackagingRelabellingRepackagingSterilisation

GMP documents matched to this site (6)

DocumentAuthorityInspectionSource
DE_BY_04_GMP_2026_0056
GMP certificate
Competent authority of Germany26 Feb 2026
within 3-year review window
EudraGMDP
DE_BY_04_GMP_2026_0109
GMP certificate
Competent authority of Germany26 Feb 2026
within 3-year review window
EudraGMDP
DE_BY_04_GMP_2025_0149
GMP certificate
Competent authority of Germany21 Jul 2025
within 3-year review window
EudraGMDP
DE_BY_04_GMP_2025_0084
GMP certificate
Competent authority of Germany12 Jul 2023
outside 3-year review window
EudraGMDP
DE_BY_04_GMP_2024_0129
GMP certificate
Competent authority of Germany12 Jul 2023
outside 3-year review window
EudraGMDP
DE_BY_04_GMP_2024_0161
GMP certificate
Competent authority of Germany12 Jul 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.