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Quality Policy
Quality Control
QC Department
QC Procedures
 

Supplier Quality Assurance
Incoming purchased parts and materials are inspected to make sure that they conform to specification/drawing requirement before releasing to stock.

Manufacturing Quality Control
Each product, parts inspection and testing shall be performed in according with COSONIC testing procedure.

QC Inspection
*Roving Inspection and Test Equipment Monitor
A three hours basis to verify the material, tools and operation procedures are adequate and results meet acceptable criteria.

*QA Outgoing Inspection
Products passed through final test will be controlled by lot acceptance sampling inspection to verify product function and packing configuration before shipping to customer.

Statistical Process Control and Analysis
* QA department will develop the statistical process control program (X-R, P, U Chart) to insure the process and product consistency.
* Production/Manufacturing engineering department to provide failure analysis and proposal of corrective action.
* QA department to follow up corrective action.

Calibration of Measuring Equipment
QA department is to determine which assigned equipments required calibration.  Measuring and testing devices are not allowed to use directly to the products without calibration. All the measuring devices and tools that are calibrated shall have a calibration card on the file, showing due date, calibration date, inspection stamp.  All measurement standards used for calibration shall have the capabilities for accuracy, stability, range and traceability to National Bureau of Standards.

Corrective Action Request
A notification of corrective action is to be given by COSONIC to related department people, subcontractors and vendors to assure the effective action is taken to remove the immediate problem symptom and to prevent recurrence of discrepancy during manufacturing.

Reliability and Failure Analysis
* Reliability
Reliability is the probability of performing without failure a specific function under given condition for a specified period of time.
We take periodically samples from current products for the life time and MTBF (Mean Time Between Failure) calculation and related items customer referred.

* Failure Analysis
The failure analysis programs are performed to find out defects causes and defects location according to the inspection or testing daily report.

Record Retention
COSONIC shall maintain a complete record of quality control actions, those data to be used as evidence of previous actions required and / or taken, those records are kept in an orderly arrangement for future reference.

Document Control
All manufacturing related documents should be signed off by authorized people to control in a manner that assures timely incorporation of design and quality requirement before issuing/control by document control center to the latest revision level.

Non-conforming Material
Non-confirming material shall be kept in special container with clear identification. A discrepant material report shall be generated and processed through the related department, then notify MRB for a material review and disposition, a corrective action report shall be generated to the responsible parties for non-conforming material.

Storage, Handling and Delivery
All the incoming material shall be marked with "pass" or "reject" labels after incoming inspection in prior to move into stockroom.
Packaging and shipment of products to customer will be properly taken as the statement in the specific orders.

 


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