MANCIN NADIA S.R.L.
Company-provided description, not an official-source fact. Certifications, capacities, years and market positions stated in it are the company's own claims until a record below confirms them.
曼辛·纳迪亚 |鱼类特产
创始人马蒂诺·德·阿戈斯蒂尼 (Martino De Agostini) 凭借古老的腌制配方（尤其是鳗鱼和凤尾鱼的腌制配方），凭借技巧和热情开始了这一职业。多年来，由于我们的研究人员始终关注市场和消费者的需求和要求，古老的传统与创新相结合。今天，马蒂诺的梦想在拥有尖端技术和系统的现代化工厂中得以延续，研究、质量和实验是真正的强项，新的厨房和美食部门也在这里诞生。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer (official record)
- Location
- Ariano Nel Polesine, Italy
- Website
- https://mancinnadia.it
- Categories
- 海鲜和水产养殖
Listed in a source registry
Italian Ministry of Health, establishments recognised under Reg. (EC) 853/2004
What is established and what is not
No researcher review has been written for this company yet. 7 official records from 6 official sources are on file. Everything is listed below with its evidence type: each entry confirms only what it literally says; none of them is a review. The manufacturing role above rests on the official records listed below, and only as far as each literally goes: a facility registration or licence is not an observation of current production. Nothing here confirms ownership or trading status beyond what each record literally says.
Facts on file, each with its evidence type
- Approved food establishment (record type: sector-licence-food) [official record; status green] Allowed to produce food under official inspection. checked 2026-09-17. Ministero della Salute, stabilimenti riconosciuti (Reg. CE 853/2004)
- Site address listed in a government regulator's register (record type: facility-registered) [official record; status green] Shows the regulator records a site of this company at a named address. A registration is not an observation of current production. checked 2026-09-17. Ministero della Salute, stabilimenti riconosciuti (Reg. CE 853/2004)
- EU VAT number valid for cross-border trade (record type: vat-valid) [official record; status green] The number is registered and active: we asked the EU VIES service and it answered yes. An invalid VAT number is the first sign an invoice comes from the wrong company. checked 2026-08-12. VIES (European Commission)
- Market access approved: European Union (record type: market-access-eu) [official record; status green] Shows the establishment is approved for the listed activities under the EU food-hygiene rules and appears in the EU list of approved establishments. It is not an import check and not an observation of current production. checked 2026-08-22. TRACES NT, European Commission register of approved establishments (DG SANTE)
- Active legal entity ID (LEI) (record type: lei-active) [official record; status green] A global identifier used in finance; an active one is renewed yearly. checked 2026-08-23. GLEIF global LEI register (golden copy)
- Sector of a state-aid measure received (record type: state-aid-sector) [official record; status green] Shows the state classified the aided work as manufacturing, which is not the same as the company's registered main activity. effective since 2026-04-21. Registro Nazionale degli Aiuti di Stato (rna.gov.it), open data
- Registry ID checks out with the state register (record type: registry-id-verified) [official record; status green] Helps confirm the company on this page is the same legal entity as in the register. checked 2026-09-10. GLEIF Global LEI record
Relationships
2 relationship(s) on file. Each line names the other party, the relationship as its source records it, and the source. A record of a relationship is not a finding about control beyond what it literally says.
Recorded in a source
- STRADA STATALE ROMEA 53, ARIANO NEL POLESINE (RO): Site named in the record, registry number UE IT 90. Ministero della Salute, stabilimenti riconosciuti (Reg. CE 853/2004)
- STRADA STATALE ROMEA 53, ARIANO NEL POLESINE (RO): Holds the site's permit, registry number UE IT 90. TRACES NT, European Commission register of approved establishments (DG SANTE)
Import rules for these goods
- US imports require the foreign facility to be FDA-registered and the importer to run a Foreign Supplier Verification Program (FSVP). US FDA