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  • Early on I stressed that each APQP is unique both between companies and within a company. The same is true of document changes. On the previous page I discussed some of the expected effects of a change to the process FMEA. Because of the differences in how companies structure their documentation it is only possible in a course document such as this to address the effect of changing one document on another. Another reason this is true is because every change to a process FMEA does not automatically require a change to, for example, the control plan. When the evaluation is made it may turn out that the ‘risk’ number (the RPN) may be low and thus may not require a control.

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