Build Product Consistency Into Every Production Gate
ANHONG's quality workflow covers incoming inspection, production checks, finished-product inspection, outgoing inspection and product-specific functional or reliability testing.
Test items, sample sizes, equipment, conditions and acceptance criteria vary by product and agreed quality plan. No universal failure-rate promise is made.
IQC, IPQC, FQC and OQC as Connected Gates
The approved specification, sample and inspection plan provide the reference for each gate.
Incoming Quality Control
Incoming materials and components are checked according to applicable requirements.
In-Process Quality Control
In-process checks monitor assembly, workmanship and production conditions.
Final Quality Control
Finished products are reviewed against agreed function, appearance and packing criteria.
Outgoing Quality Control
Outgoing inspection verifies shipment readiness against the project plan.
Match Testing to Product Risk and Specification
Availability, conditions and criteria must be confirmed for the selected product and project.
Functional testing
Display, camera, audio, controls, connectivity and applicable functions.
Aging testing
Product-specific powered operation or aging procedure where applicable.
Temperature testing
Applicable high- and low-temperature conditions based on the test plan.
Vibration and transport
Packaging or product checks relevant to handling and delivery risk.
Plug and button cycling
Applicable durability checks for connectors, controls and moving parts.
Packaging inspection
Contents, labels, artwork, barcode, accessories and carton requirements.
Use Real Images With Test Names and Conditions
Connect Materials, Production and Shipment Records
Traceability depth should be defined by the product, project and customer requirements. The goal is to support investigation and corrective action with identifiable records.
Material records
Applicable supplier, lot and incoming inspection information.
Production records
Configuration, work order and in-process quality information.
Test records
Applicable functional, aging or reliability results.
Shipment records
Final inspection, packing and delivery references.
Analyze, Correct and Verify
A structured corrective process matters more than an unsupported absolute quality claim.
Containment
Identify affected material, work-in-process or finished goods.
Root-cause analysis
Review product, process, material, test and configuration evidence.
Corrective action
Define responsible actions and update controls where required.
Verification
Confirm whether the action addresses the identified cause.
Communication and follow-up
Share agreed records and monitor subsequent production where applicable.
Quality Records and Market Documents Are Model-Specific
Factory-system certifications and product compliance documents serve different purposes. Product support must be mapped to the exact model, configuration and destination market.
Request the Applicable Quality Process Information
Share the model, market and quality concerns so the relevant process, test and inspection information can be discussed.