Product identity
- Buyer and supplier model codes
- Drawing and specification revision
- Included parts and accessories

Build the order around an approved specification, reference sample and agreed inspection plan. The objective is not a broad promise of “good quality,” but a traceable way to define, check and resolve the characteristics that matter for each product.
A product image cannot define dimensions, construction, finish variation, hardware, functions or packing. Before production release, the parties should identify the records that describe the accepted configuration.
The exact sequence depends on the model, materials and order risk. The quality plan should state which checks apply, who records them and what happens when a result is outside the approved requirement.
Confirm the identity and condition of specified boards, surfaces, glass, hardware, basins, electrical components and packaging materials before they are used.
Review the first production-representative unit against the current drawing, component schedule and approved appearance reference before wider production continues.
Check characteristics that are difficult to correct later, such as machining positions, edge treatment, finish preparation, assembly alignment and controlled component use.
Verify selected or agreed units for model identity, workmanship, dimensions, operation, accessories, labels and consistency with the released specification.
Confirm protection, carton identity, contained parts and order quantities, then close open inspection issues before shipment authorization.
A vanity, illuminated mirror, basin and tap do not share one universal checklist. The inspection record should refer to the exact model, option set and destination brief.
Check overall size, critical openings, basin and tap positions, plumbing zones, wall clearances and mounting points against the released drawing and agreed tolerance.
Confirm declared substrates, surfaces, edge details, hardware and controlled components using product records and traceability appropriate to the order.
Review colour, sheen, texture, grain direction, alignment, gaps, chips, scratches and visible repairs under agreed viewing conditions and reference limits.
Operate doors, drawers, controls and specified features. Check included fittings, usable clearances and product-specific functions by the agreed method.
Match model, carton and instruction information to the order. Product reports or declarations should be checked for holder, model scope, configuration and validity.
Review surface contact, corner and glass protection, secured moving parts, contained hardware, carton construction, orientation and shipment labels.
Correction of one visible defect does not necessarily prevent repetition. The response should identify the affected scope, disposition and evidence needed to close the issue.
Record the model, order, location, requirement, observed result and supporting photograph or measurement without assuming a cause.
Identify affected materials, work in progress or finished units and prevent unreviewed products from moving to the next stage.
Agree rework, replacement, acceptance by written deviation or rejection, including who can authorize the disposition.
Check the correction and any process action, then connect the closure record to the affected batch and future repeat-order reference.
Any proposed change to a controlled material, component, dimension, finish, function, label or package should be submitted before use. The request should explain the reason, affected models, technical and visual impact, document impact and evidence required for approval.
The appropriate record depends on risk and commercial agreement. It should allow the buyer and supplier to identify the product, reference, result, issue and disposition without reconstructing the order from unrelated messages.
See the project sourcing workflowA supplier cannot resolve an unstated room interface, local requirement or appearance expectation. Buyers should provide current information and name the people authorized to approve samples, changes and deviations.
Provide destination, product scope, quantities, drawings, room interfaces, finish references, documentation needs and target decision dates.
Return consolidated comments, identify the approved revision and avoid conflicting instructions from separate project participants.
Confirm applicable regulations, wall and service conditions, installation methods, receiving, storage and site inspection with qualified parties.
Include the destination, quantities, drawings, finish references and the characteristics your team needs to approve. The next discussion can then focus on the appropriate sample, inspection and record plan.