Incoming review
Check relevant ingredients, packaging materials, identification and approved supplier information.
Quality control starts with an approved product and packaging specification—not a generic list of tests. LaiZhi coordinates project-relevant incoming, in-process, packaging and finished-product requirements with the assigned production facility.
The inspection plan should reflect the formula, process, package, buyer requirements and applicable destination conditions. Test items, methods, sampling and acceptance criteria must be agreed before they are treated as order requirements.
This distinction matters: a facility may have broad inspection capability, but the exact checks and reports supplied with an order remain project-specific.
Check relevant ingredients, packaging materials, identification and approved supplier information.
Monitor agreed production parameters and record project-relevant observations.
Review container, closure, artwork, coding, seal or seam and packout as applicable.
Assess the agreed finished-product attributes and batch records before release.
Connect controlled materials, formula version, batch, inspection and packing records.
Record deviations, assess disposition and communicate relevant corrective actions.
Package inspection may include dimensions, container condition, closure match, seal or seam review, leakage checks, artwork and coding. The applicable method and acceptance criteria must be confirmed for the selected format.
| Review area | What to verify |
|---|---|
| Incoming materials | Identity, batch information, condition and packaging specification |
| Processing | Controlled parameters and project-relevant in-process observations |
| Filling & closure | Fill-related checks, container condition and seal or seam review as applicable |
| Coding & artwork | Approved version, legibility, placement and pack identification |
| Finished product | Agreed physical, sensory, chemical or microbiological review |
| Packing & release | Case, label, quantity, pallet and release records |
Identify formula, material and packaging versions.
Link production details to a traceable batch.
Capture agreed incoming and in-process results.
Assess the batch against release requirements.
Link case, pallet and shipping identification.
Provide the agreed project documentation.
The applicable checks are defined by the approved product, process, package and buyer requirements. They may include incoming, in-process, packaging and finished-product review, but the exact scope must be confirmed for each project.
Yes. State the required test, method, acceptance criteria, reporting format and destination requirement during project review so availability and responsibility can be confirmed.
The agreed route should connect controlled materials and packaging, formula version, production batch, inspection status, packing identification and shipment records.
No. A management-system or facility certificate does not replace product-specific specifications, process controls, inspections or release requirements.
A buyer may request third-party inspection or testing. Scope, timing, access, cost and acceptance criteria should be agreed before production or shipment.
Use the connected capability pages to verify development, manufacturing, quality, facility, document and export requirements before order release.
Capability, facility, certification, testing, quantity, schedule and document availability are confirmed for each approved project.
Send the target specification, packaging format, required checks, acceptance criteria, reporting needs, destination and third-party inspection requirements.
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