Documented Production Environment
Review what the supplied facility, equipment and historical management-system records support, then identify the current evidence needed for a specific order.
What is directly documented
The source set contains photographs of a Tengyao-branded facility, equipment, line activity, workshop space and other production-area scenes. The registered company is Huai'an Tengyao Packaging Co., Ltd., unified social credit code 91320826695545110B.
The registered address shown in the supplied Chinese records is No. 2 Wei 6th Road, West Zone, Lianshui Economic Development Zone, Huai'an, Jiangsu 223400, China.
What must still be confirmed per project
The archive does not prove that every glass bottle, closure, accessory or decoration process is made inside the same facility. Buyers should request the sourcing map, current audit evidence and responsible production site for the exact quoted model.
Review the quality evidence boundaryThe historical scope was limited
The supplied QMS and EMS records covered production of aluminum bottles and injection-molded parts within cosmetic packaging, and both expired on 10 February 2025. This history cannot be extended to every glass bottle, closure, accessory or decoration process.
Operational photographs in the supplied archive
Read this sequence as documentary evidence of place and equipment, not as a claim that every catalog category follows one production route. Captions state the exact buyer question each image can support.
A recommended order-control sequence
- 01
Scope and sourcing map
Identify the primary container, functional components, decoration and pack-out owner.
- 02
Current technical evidence
Collect model drawings, materials, site details and applicable valid documents.
- 03
Sample and test plan
Approve the assembled package against formula, function, appearance and transit needs.
- 04
Production controls
Record critical dimensions, color, decoration, component fit and inspection method.
- 05
Packing and release
Confirm pack-out, labels, carton protection, documentation and shipment release criteria.
Factory due-diligence questions
- Which legal entity and site will produce or assemble each component?
- Which steps are internal and which are sourced?
- Which current audits, licenses or certificates apply to that site and scope?
- How are incoming components, process controls and final release recorded?
- Which approved sample, drawing and inspection method govern the order?
Continue the qualification path
Use the quality page for historical document status, then add current factory and product evidence requirements to the RFQ.
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