VUAB Pharma A.S.

Roztoky, Czech RepublicFEI 3003002370API manufacture registered

VUAB Pharma A.S. is a drug establishment in Roztoky, Czech Republic, registered with the US FDA under FEI 3003002370. Its registered operations are: API manufacture. 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.

API manufacture

GMP documents matched to this site (6)

DocumentAuthorityInspectionSource
sukls399701/2025
GMP certificate
Competent authority of CZECHIA4 Dec 2025
within 3-year review window
EudraGMDP
sukls399713/2025
GMP certificate
Competent authority of CZECHIA4 Dec 2025
within 3-year review window
EudraGMDP
sukls189367/2024
GMP certificate
Competent authority of CZECHIA11 Sept 2024
within 3-year review window
EudraGMDP
sukls73585/2023
GMP certificate
Competent authority of Czechia6 Apr 2023
outside 3-year review window
EudraGMDP
sukls162469/2022
GMP certificate
Competent authority of Czechia15 Sept 2022
outside 3-year review window
EudraGMDP
sukls162566/2022
GMP certificate
Competent authority of Czechia15 Sept 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.