PRODITEC SAS
1987 में स्थापित, प्रोडिटेक फार्मास्युटिकल और मिंटिंग उद्योगों के लिए स्वचालित दृश्य निरीक्षण समाधान का अग्रणी निर्माता है। यूरोप, एशिया और
1987 में स्थापित, प्रोडिटेक फार्मास्युटिकल और मिंटिंग उद्योगों के लिए स्वचालित दृश्य निरीक्षण समाधान का अग्रणी निर्माता है। यूरोप, एशिया और उत्तरी अमेरिका में 3 कार्यालयों के साथ, और
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Pessac, France
- Founded
- 1987
- Website
- proditec.com
- Categories
- फार्मास्युटिकल विनिर्माण
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)