Factory defective product management, do not accept good products, do not manufacture defective prod

It should be analyzed from several aspects.

One is unexpected, that is, you don't plan to let it go out but it goes out, which is generally caused by loopholes in the design of the shipment inspection, such as the sampling system is not too reasonable, or there are some performance parameters that are missed.

The other is expected, that is, the inspection is unqualified, but the company proceeds from its own interests, taking into account the customer's requirements for product quality parameters, and believes that it should be able to meet the customer's requirements, and then release it as a qualified product. Or it is leaked after consultation with the customer.

The specific situation has to be analyzed according to the actual situation of the company.

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Summary. Hello, happy to answer this question for you.

This is the "three noes" principle of process control.

2. Do not manufacture defective products: the work of this process should be clear and the inspection specifications should be clarified to avoid bad phenomena.

3. Do not flow out defective products: when defective products have been generated, they should be isolated and corresponding measures should be taken to solve them.

What does it mean not to accept good products, not to manufacture defective products, and not to flow out defective products?

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Hello, happy to answer this question for you. This is the "three noes" principle of process control. 1. Do not accept defective products

The next process that can be established is the customer relationship, and the next process has the right to reject nonconforming products in the previous process and establish a process of mutual inspection. 2. Do not manufacture defective products: The work of this process should be clear to check the resistance and rapid difficulty to inspect the Changyu specifications to avoid undesirable phenomena.

3. Do not flow out defective products: when defective products have been generated, they should be isolated and corresponding measures should be taken to solve them.

The above is a question you are asking, I hope it will be helpful to you.

Legal analysis: The State Food and Drug Administration is in charge of the reporting and monitoring of adverse drug reactions nationwide, and the local drug regulatory departments at all levels are in charge of the reporting and monitoring of adverse drug reactions within their respective administrative areas. Health administrative departments at all levels are responsible for the management of medical institutions within their respective administrative areas related to the implementation of the adverse drug reaction reporting system.

Local drug regulatory departments at all levels shall establish and improve adverse drug reaction monitoring institutions, which are responsible for the technical work of adverse drug reaction reporting and monitoring within their respective administrative regions.

Legal basis: Criminal Law of the People's Republic of China

Article 140: Where a producer or seller adulterates or adulterates a product, passes off a fake product as genuine, shoddy or passes off a substandard product as a qualified product, and the sales amount is between 50,000 and 200,000 RMB, he shall be sentenced to fixed-term imprisonment of not more than two years or short-term detention and/or a fine of not less than 50 percent but not more than two times the sales amount;

where the sales amount is between 200,000 and 500,000 RMB, a sentence of between two and seven years imprisonment is to be given, and a concurrent fine of between 50 and 2 times the sales amount is to be given; where the sales amount is between 500,000 and 2,000,000 RMB, a sentence of 7 or more years imprisonment and a concurrent fine of between 50 and 2 times the sales amount is to be given;

where the sales amount is more than 2,000,000 RMB, the sentence is 15 years imprisonment or life imprisonment, and a concurrent fine of between 50% and 2 times the sales amount or confiscation of property.

Article 141: Where the production or sale of counterfeit drugs is sufficient to seriously endanger human health, a sentence of up to three years imprisonment or short-term detention is to be given, and/or a fine of not less than 5 percent but not more than 10 times the amount sold; where serious harm is caused to human health, a sentence of between three and ten years imprisonment and a fine of between 50% and 2 times the amount of sales is to be given;

and where death is caused or especially serious harm to human health is caused, a sentence of 10 or more years imprisonment, life imprisonment or death is to be given, and a fine of between 50 and 2 times the amount of sales or confiscation of property is to be given.

Defective products refer to raw materials, semi-finished products and finished products that do not meet the relevant quality requirements in manufacturing. Among them, the quality requirements can be the inspection quality requirements of the inspection, the quality requirements of the manufacturing process, the quality requirements of customers, and the provisions of national laws and regulations.

When it is found that it is unqualified, or when the worker's self-inspection or the inspection of the production supervisor is found to be unqualified, the operator (or operator) should be immediately required to isolate and mark the unqualified products. and notify the supervisor of the quality control department. The supervisor of the quality control department should immediately go to the site for analysis and judgment.

When the analysis determines that the disconformity found is a coincidental nature, the number is small, the nature is not serious, and the impact is not large, such minor nature of the unqualified can be directly disposed of by the quality control officer or quality control supervisor. The methods of disposal include rework, repair, scrapping, etc.

When the quality control supervisor analyzes and judges the quality accident to be of a serious nature (serious; Refers to a non-conformity other than the above-mentioned minor non-conformity. As; Large quantity, large loss, large impact, rebirth, serious nature, etc.), the responsible person should be notified to do a good job of isolation of nonconforming products, and notify the quality control staff to make a good mark. At the same time, immediately organize production technicians to dispose of it.

Disposal methods include rework and repair, full inspection and selection, scrapping, etc.

Summary. <>

Hello friends, the answer is as follows:1Help with the job:

The defective product control process can effectively help enterprises improve product quality and customer satisfaction, reduce the rate of defective products, reduce unnecessary costs and losses, and thus enhance the market competitiveness of enterprises. 2.Practical Status:

The defective product control process is actually applied to the production and chain management of the enterprise, involving multiple links, including quality control, supervision and sampling, quality inspection and supervision, failure analysis, corrective and preventive measures, etc. The key is to develop a control process that is suitable for the company and to continuously optimize and improve it to ensure its effectiveness and sustainability.

How does the defective product control process help the work?

Hello friends, the defective product control process can help enterprises find product quality problems in time and correct and improve, so as to reduce the rate of defective products, avoid losses and increase the complaint rate, and improve the reputation of the brand and customer satisfaction. In addition, the defective product control process can help companies control production costs more effectively, improve production efficiency and profit margins.

Please answer the following two questions, the first of which will help you in your work. , the second practical application situation, the answer should be simple and clear, and be able to say the main point.

Hello friends, the answer is as follows:1Help with the job:

The defective product control process can effectively help enterprises improve product quality and customer satisfaction, reduce the rate of defective products, reduce unnecessary costs and losses, and enhance the market competitiveness of enterprises. 2.Practical Status:

The defective product control process is actually applied to the production and chain management of the enterprise, involving multiple links, including quality control, supervision and sampling, quality inspection and supervision, fault fiber chain analysis, corrective and preventive measures, etc. The key is to develop a control process that is suitable for the company and to continuously optimize and improve it to ensure its effectiveness and sustainability.

Why don't you say it, I'm paying for it.

Hello friends, the answer is as follows:1Help with the job:

The defective product control process can effectively help enterprises improve product quality and customer satisfaction, reduce the rate of defective products, reduce unnecessary costs and losses, and enhance the market competitiveness of enterprises. 2.Practical Status:

The defective product control process is actually applied to the production and chain management of the enterprise, involving multiple links, including quality control, supervision and sampling, quality inspection and supervision, fault fiber chain analysis, corrective and preventive measures, etc. The key is to develop a control process that is suitable for the company and to continuously optimize and improve it to ensure its effectiveness and sustainability.

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