Product NC documentation
Product NC documentation is prepared for managing records of non conformance identified in manufacturing processes with product concern.
Product NC documentation is established by quality department to recording product non conformance during the inspection at various stages of organization, raw materials, in-process and final inspection process outputs can be final product and non conformance product or rejected, the process of product NC and its concern documentation describe the details of product non conformance and reasons to acknowledge the concern peoples to implement the quality of product accordingly. The product non conformance can be raised in any stage of manufacturing processes, when the quality team is verify the processes, manufacturing stages, raw materials, process activities that in during the inspection, any product concern non conformance is identified that quality team is remark the product details and record product non conformance as per product described in the job card.
The product non conformance (NC) documentation is prepared by quality department, quality engineers are responsible for conduct the product quality inspection hence the team is verify the raw materials, in-process inspection and final product inspection, during the inspection process in case any product having a issues, defects or not acceptable as per product standards / acceptable criteria that the product is considered in rejected category or product non conformance are managed as separate for further actions. The documentation for each product non conformance identified are provided to concern department for further actions hence the documentation is part of communication with departments to identifications of product non conformance, sources of cause and actions plans are conducted according to product non conformance summary report. See picture below provided example format:
Product non conformance summary format is used to recording information of all the product non-conformance identified during the inspection process, during the manufacturing activities, and on final stages of the quality inspection is covered. The product NC reporting and its records are managed by quality department and responsible for identification of quality of product during the manufacturing and final quality inspection processes. The each identified non conformance is managed in the summary sheet and discuss with the production peoples for elimination of rejection, defects due to machinery, equipment or processes are conducted and implemented effective plans on as outputs of discussions. The documentation are managed as per standard documentation system.
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Product non conformance summary
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