PRODITEC SAS
Fundada em 1987, a Proditec é fabricante líder de soluções automatizadas de inspeção visual para as indústrias farmacêutica e de cunhagem
Fundada em 1987, a Proditec é fabricante líder de soluções automatizadas de inspeção visual para as indústrias farmacêutica e de cunhagem. Com 3 escritórios na Europa, Ásia e América do Norte, e
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Pessac, France
- Founded
- 1987
- Website
- proditec.com
- Categories
- Fabricação farmacêutica
Listed in a source registry
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- domain-registered (green), checked 2026-08-20 Domain registry record
- registered-since (green), effective since 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- facility-registered (green), effective since 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- export-registered (green), checked 2026-09-03 EU EORI validation (European Commission)
- registry-activity (green), checked 2026-07-30 INSEE Sirene (annuaire-entreprises)
- registry-id-verified (green), checked 2026-07-30 INSEE Sirene (annuaire-entreprises)
- directors-on-file (green), checked 2026-07-30 INSEE Sirene (annuaire-entreprises)
- debarment-clear (green), checked 2026-07-30 OpenSanctions
- web-presence-since (green), checked 2026-08-21 Internet Archive (Wayback)
- sanctions-clear (green), checked 2026-07-30 OpenSanctions
- registry-active-global (green), checked 2026-07-30 INSEE Sirene (annuaire-entreprises)
- workforce-on-record (green), effective since 2026-07-01 INSEE SIRENE (Registre national des entreprises)
- vat-valid (green), checked 2026-07-30 VIES
Import rules for these goods
- Medicines imported into the EU must come from a site holding an EU GMP certificate, and the importer needs a manufacturing/import authorisation. European Medicines Agency (GMP)