Potential failure mode and effect analysis (FMEA) Course Background: Potential defects mode and effects analysis (FMEA) is a pre-production process, the analysis of prevention work, engineering and technical personnel from the design stage through analysis and evaluation of relevant processes listed possible defects and consequences for the actual design, production and assembly of prevention, through continuous assessment, verification and improvement, the product tends to be the best, and ultimately the maximum guarantee products to meet customer requirements and expectations. Course objectives: one, to understand the function and production requirements FMEA two master FMEA method and applied to the improvement of business activities 3, master FMEA dynamic management requirements, reduce the incidence of defective products, to enhance the competitiveness of enterprises Course Outline: l FMEA ◎ FMEA concepts and understanding the history and current situation; ◎ FMEA of the definition, purpose and classification; ◎ FMEA implementation timing. l FMEA terminology used ◎ control plan; design intent; design life ◎ design validation / verification; experimental design; ◎ arrangement diagram (Plato); ◎ performance; process; process changes; ◎ Quality Function Deployment; special characteristics of the product; l ◎ FMEA FMEA work flowchart diagram with causal relationship analysis; ◎ FMEA work flow analysis; l FMEA implementation of the detailed steps ◎ FMEA form filling requirements of each part of the description; ◎ severity evaluation criteria; ◎ failure resulting frequency evaluation criteria; ◎ failure probability evaluation criteria were found; various types and characteristics of the FMEA analysis process characteristics; l Process FMEA Ten Steps Detailed ◎ produced object recognition and target; ◎ process performance standards; ◎ process of requirements; ◎ processing Process block diagram; ◎ Expand adverse schema items; ◎ The key is to focus on items due; ◎ column adverse presumption reasons; ◎ risk coefficient determined; ◎ bad pattern grading; ◎ reduction factor re-assessed. l FAQ Making Process FMEA analysis and countermeasures ◎ mode enumeration of potentially fewer projects; ◎ process commenced with the flowchart confusion; ◎ mistake because when the defective mode content; ◎ no severity assessment of the severity factor; ◎ coefficient of frequency of occurrence assessment unfounded; ◎ detection probability proportional coefficient assessment; ◎ proposed measures proposed only recognize the degree of risk; ◎ Improved assessment after three degrees do not correspond; ◎ FMEA form and fill terminology wrong;