Verify the facility and scope in the issuer's own database.
Sucotond USA is the Brooklyn sales and project-coordination office. Manufacturing is handled by Sucotond (Guangzhou) Health Biotechnology Co., Ltd., which was found in NSF's public 455-2 GMP listing as a Manufacturing Facility with product category Gummy during the latest recorded check.
The dated record includes the exact source, check time, listed address, technologies and evidence limitations. Other registrations or certificates should not be relied on until the current source document, holder, site, scope and validity are reviewed.
Public VerificationWhat is verified publicly—and what still needs source documents
A supplier-qualification decision should distinguish an issuer-controlled public listing from badges, screenshots and unsupported website statements.
Public NSF listing
The current NSF listing identifies the Guangzhou legal entity, manufacturing-site address, manufacturing-facility type and Gummy product category.
Listed technologies
The same listing shows baking, mixing, molding, packaging/labeling, quality-unit operations and warehousing. Confirm applicability to the proposed SKU.
Not product approval
A facility listing does not approve a formula, label, health claim, finished batch, destination market or shelf-life statement.
Other facility documents
Current FDA registration, HACCP, ISO 22000, BRCGS or other status must be verified from the applicable source document before it is represented for a project.
Project-specific evidence
Define ingredient identity, formula specification, release tests, batch documents, packaging and stability support separately. Use the COA and batch-records checklist to compare the layers.
Controlled document sharing
Availability depends on document-owner approval, issuer terms, the relevant facility and the specific project scope.
A practical document sequence
Use the printable 24-point supplier qualification checklist to record the evidence and open gaps. Before matching documents, review the separate Brooklyn office and Guangzhou manufacturing-facility roles.
1. Match legal identity
Use the exact factory name and manufacturing-site address.
2. Check the issuer
Prefer the issuing body's public database or direct verification route.
3. Check scope
Confirm the site type, product category and activities covered.
4. Check validity
Request the current document rather than relying on an old image.
5. Map to the project
Identify which facility, formula, process and package apply to the SKU.
6. Retain batch evidence
Agree the finished-product COA, lot identity and supporting records.
Need current facility documents for an active project?
Send the company name, target product and document checklist to the Brooklyn project office. Requests are handled in the context of an active qualification or manufacturing discussion.
The jump uses a browser text fragment. If your browser opens the full directory without jumping, use Find and search the exact legal name: Sucotond (Guangzhou) Health Biotechnology Co., Ltd.