Review real factory evidence, the documented manufacturer, quality-management scope and the route from project inputs through assembly, debugging and acceptance planning.
Keep the public brand, document entity and contracting responsibility explicit.
AIX PACK is the public commercial brand used on this website. The audit and certificate evidence shown here is issued to Guangdong Kinghanlong Intelligent Equipment Technology Co., Ltd. Entity names are reproduced exactly as stated in each document, and the quotation identifies the contracting entity and project responsibilities.
Each real image carries its source, date and evidence boundary.
A dated production route is evidence; final scope and acceptance remain project-specific.
Material behavior, dose or fill range, pack, film, output basis, market, utilities and downstream boundary.
Freeze the machine and line scope, interfaces, documents and project-specific verification basis.
Define parts-processing and procurement responsibilities without inferring an unsupported in-house share.
Mechanical assembly, electrical integration and interface checks follow the confirmed project route.
Use agreed inputs, observable checks and records; visible audit evidence is not a project acceptance result.
The signed project scope assigns FAT, deviations, sign-off, delivery and handoff responsibilities.
Audit, assessment and QMS certification answer different questions.
Manufacturer status and the recorded material, machining, assembly, debugging/testing, packaging and inspection route at the audit date.
Not an SGS product certificate, model certificate, performance guarantee or perpetual capacity statement.Packaging-machinery production, parts processing, assembly, debugging, production management and inspection context; document-stated validity 2025-12-09 through 2026-12-08.
Not a product certificate, passed FAT, universal service territory, availability or result.
The certificate states that Guangdong Kinghanlong's quality-management system is certified to ISO 9001:2015 for the production of packaging machines, certificate 98926Q0112R153, subject to ongoing surveillance.
Does not certify a machine model, output, accuracy, GMP, FDA, CE, validation or customer project.Define applicable requirements and responsibility before turning a document request into a claim.
Destination market, product and contact risk, required standards and validation expectations.
Available design, material, electrical, traceability, test and document scope for the project.
Contact-material evidence, surface and cleaning requirements, test protocol, acceptance criteria and DQ/IQ/OQ/PQ responsibilities where applicable.
GMP, FDA, CE and validation are buyer- or project-defined requirements to verify; they are not company-wide or machine-wide approvals on this page.
Keep material feasibility, manufacturing evidence and formal FAT responsibilities in their proper routes.
Representative product, film and trial-pack questions belong to Sample Testing.
Plan Sample TestingInputs, conditions, checks, records, deviations and sign-off responsibilities belong to Service & Support.
Define the FAT and service scopeReview primary equipment, downstream modules, utilities, access and third-party boundaries together.
The visible answers are the only FAQ structured-data source.
AIX PACK is the public commercial brand used on this website. Third-party reports identify Guangdong Kinghanlong Intelligent Equipment Technology Co., Ltd. as a manufacturer and record packaging-machine production processes. Entity names are reproduced exactly as stated in each document, and the quotation identifies the contracting entity and project responsibilities.
No. QIP-ASR2511099 is a dated SGS audited-supplier report and 483515454_P+T is a TÜV Production and Trading Assessment. They provide third-party evidence but are not product certificates or universal performance approvals.
Certificate 98926Q0112R153 states an ISO 9001:2015 quality-management-system scope for the production of packaging machines, subject to ongoing surveillance. It does not certify a specific machine model, output or customer project.
AIX PACK can review the destination market, contact materials, cleaning, traceability, electrical documents, test records and validation responsibilities required for a project. The applicable scope must be confirmed in project documents; this page does not claim that every machine is GMP-, FDA- or validation-approved.
Manufacturing and debugging evidence show the documented production route. The project service scope separately defines any Factory Acceptance Test inputs, conditions, checks, records, deviations and sign-off responsibility, while Sample Testing owns material feasibility and trial-pack questions.
Send product behavior, dose or fill range, pack dimensions, film, stable-output target, destination market, required documents, utilities, layout and any inspection, counting or cartoning scope.
We will separate visible manufacturer evidence from project-defined engineering and acceptance responsibilities.
