Export Desk: Private Label · OEM · B2B Manufacturingasapharmavet@gmail.com · +90 530 349 6582
DOCUMENTED, CURRENT & SCOPE-SPECIFIC

Quality documentation buyers can review.

We make current management-system certificates available with their stated scope. Product eligibility, label claims, importer duties and destination-market registration are assessed separately for each export project.

Available company documentation

Current certificates for the stated scope.

These files relate to wholesale activities in animal-feed products, as written on each certificate. They are not presented as U.S. FDA registration, U.S. market authorization, product approval, FSMA compliance or pet-supplement manufacturing certification.

01
QUALITY MANAGEMENT

ISO 9001:2015

Quality Management System certificate, issued to Asa Pharma İlaç Veterinerlik Turizm Ticaret Ltd. Şti. for the stated animal-feed wholesaling scope.

Certificate: W-25052-QValid to: 01 May 2027
Open certificate ↗
03
CUSTOMER SATISFACTION

ISO 10002:2018

Customer Satisfaction Management System certificate, issued to Asa Pharma İlaç Veterinerlik Turizm Ticaret Ltd. Şti. for the stated animal-feed wholesaling scope.

Certificate: W-260453-CValid to: 04 May 2027
Open certificate ↗
How buyers can use the documents

Read the issuer, legal entity, validity and scope together.

A certificate can support company due diligence when its issuer, named legal entity, certificate reference, dates and scope are recorded accurately. Keep that company evidence separate from a product specification, a batch file, a destination registration or an importer’s customs requirement.

Document review questions.

Which legal entity is named?
What exact activity does the scope describe?
What is the certificate reference and validity?
Which SKU and country questions remain open?
Who owns importer or broker verification?
Company evidence vs. market entry

Quality documents are one part of a project file.

For a private label or export project, the buyer may also need product and packaging information, ingredient or composition details where relevant, label and claim review, testing or batch evidence, commercial documents, origin and transport inputs and importer-specific records. The exact file is defined by the selected SKU, country and transaction.

Information ASA Pharma Vet can organize

Company-level certificate copies, project brief inputs, format and packaging discussion, agreed product information, sample and quote scope, and the handoff questions that need to be answered before production or shipment.

Review the Private Label route

Information the destination must confirm

Classification, ingredients, claims, label acceptance, local registration, importer responsibilities, customs documents, state or local requirements and any product-specific shipment conditions. These are not established by the three certificates above.

Read the documentation checklist

Important: A management-system certificate does not replace product classification, ingredient review, FDA facility registration, importer FSVP obligations, state registration, customs review or claim approval in a destination market. Verify the actual SKU and shipment with the responsible importer and qualified advisers.
QUALIFIED B2B ENQUIRY

Send the document request with the product brief.

Include country, buyer company, sales channel, format, packaging, expected volume, target timing and the documents requested by the importer or broker.

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