AVT Natural Products Ltd
AVT Natural Products produz oleorresina de calêndula e ésteres de luteína, oleorresinas de especiarias e essências…
AVT Natural Products produz oleorresina de calêndula e ésteres de luteína, oleorresinas de especiarias e óleos essenciais para as indústrias globais de nutracêuticos e corantes alimentícios. Operando fazendas integradas e instalações de extração em Kerala e Tamil Nadu, a empresa controla a qualidade desde a semente até o extrato final. Os contratos de atacado em massa são apoiados pela certificação ISO 22000, credenciais orgânicas do USDA e equipes dedicadas de documentação de exportação para requisitos regulatórios norte-americanos, europeus e japoneses.
- Type
- Manufacturer
- Location
- Kochi, India
- Founded
- 1987
- Website
- avtnatural.com
- Categories
- Alimentos gourmet e especialidades, Suprimentos médicos e de saúde
- Markets
- Estados Unidos, Alemanha, Japão, Países Baixos, Austrália
Verified facts
- lei-active (green), checked 2026-08-07 GLEIF global LEI register (golden copy)
- web-presence-since (green), checked 2026-08-03 Internet Archive (Wayback)
- debarment-clear (green), checked 2026-08-04 OpenSanctions
- sanctions-clear (green), checked 2026-08-04 OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-04 Mail server of the company domain
- domain-registered (green), checked 2026-08-04 Domain registry record
Claimed certifications
- ISO 22000, Food Safety IAF CertSearch
- HACCP
- USDA Organic USDA Organic INTEGRITY
- Halal Certified
Import rules for these goods
- EU imports of food of animal origin and many other food categories must be pre-notified in TRACES and enter through border control posts. European Commission (TRACES)
- US imports require the foreign facility to be FDA-registered and the importer to run a Foreign Supplier Verification Program (FSVP). US FDA
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)