PPAP讲义.ppt
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1、生产件批准程序Production Part Approval Process,Conduct PPAP 生产件批准程序对每种零(部)件, 要求供方在向顾客(三大汽车公司)发运第一批产品之前进行Prior to the 1st Production Batch Supply to CustomerFor Each Part Number,顧客呼聲Voice of customer,特殊特性 S.C,可行性評審 Feasibility Review,產品設計及DFMEA DFMEA & Product Design,樣機控制計劃 Prototype C.P,過程設計及PFMEAPFMEA & P
2、rocess design,試生產控制計劃 Prelaunch C.P,MSA研究 MSA Study,初始能力評估及過程確認Process validation & capability Study,設計輸出 Design Output生產控制計劃 Production C.P,生產 Production,特續改進 Continuous improvement,統計技術 SPC,統計技術 SPC,PPAP submission , PPAP呈交,A P Q P產品先期策劃,Mistake Proofing 防錯方法,生产件批准程序 PPAP,对所有生产、服务产品和散装材料都要求 生产件批准F
3、or all production, services and bulk material, needs approval 提交的部件需取自有效的生产过程 Submission is from the valid production process 有效生产过程包括: 一小时到一个班次的生产 Production from one hour to one shift规定的产量至少为 300件 Minimum production is 300 pieces每一腔都应进行 For each cavity,生产件批准程序 PPAP,目的 Purpose了解顾客所有要求 To understand
4、 all customer requirements具有潜在能力 (Cpk/PpK)Have sufficient capability (Cpk/PpK)生产节拍满足要求 Production rate is sufficient,生产件批准程序 PPAP,以下列情况出现时, 需在首批产品出货前提交 PPAP:When the following conditions show up, start PPAP process新部件或产品 New component or product2.经修正不合格项目後所生产的产品 Rectification of the nonconforming pr
5、oduct3.根据工程更改而修改的产品Products have engineering changes当对PPAP的需求有怀疑时, 联络相关顾客的批准部门 If in doubt of PPAP, contact customer approval responsible department,需编制的文件/项目Document/ Item shall be prepared,无论是否提交供应商必须完成和编制下述19 份文件No matter the documents have to be submitted, 19 records have to be ready:1.所有顾客和供应商设
6、计记录all design records from customer and supplier必须具备所有的可销售产品设计记录,包括:部件水平。 shall have all design records for the saleable product, including components level. 若设计记录,如CAD/CAM是以电子版形式存在,供方必须制作一份硬件拷贝来确定所进行的测量。 Where the design record, e.g. CAD/CAM is in electronic format, supplier shall produce a hard co
7、py to identify measurements taken.,需编制的文件/项目Document/ Item shall be prepared,2.授权的工程更改Authorized engineering changes供方必须具有尚未记入设计记录中,但已在产品,零件或工装上体现出来的任何授权的工程更改文件。 supplier shall have any authorized engineering change documents not yet recorded in the design record but incorporated in the product, par
8、t or tooling. 3.客戶工程批准 Customer Engineering Approval在设计记录有规定时,供方必须具有顾客工程批准的证据。Where specified by the design record, the supplier shall have evidence of customer engineering approval.,需编制的文件/项目Document/ Item shall be prepared,4.设计FEMA (有设计时) DFMEA (have design)5.制程流程图 Process Flow Diagram必须具备清楚描述生产过程
9、的步骤和次序的过程流程图。 shall have a process flow diagram clearly describes the production process steps and sequence. 6.制程FEMAPFMEA,需编制的文件/项目Document/ Item shall be prepared,7.尺寸测量 Dimension Measurement必须提供设计记录和控制计划要求的尺寸验证。 provide evidence that dimensional verifications required by the design record and the
10、 Control Plan .结果表明符合规定要求的证据。 results indicate compliance with specified requirements. 对每一个的加工过程,如:单元或生产线和所有的型腔、模型、样皮或冲模,必须有尺寸结果。shall have dimensional results for each unique manufacturing process, e.g. cells or production lines and all cavities, molds, patterns or dies.,生产件批准程序 PPAP需编制的文件/项目,8.按设计
11、记录规定的材料, 性能和耐久性试验结果Test results- material, functional and performance關於設計記錄或控制計劃中規定的試驗,必須有材料和/或性能試驗結果的記錄。 Shall have records of material and/or performance test results for specified on the design records or Control Plan. 9.制程能力评估结果 Results of capability在提交由顾客或供方指定的所有特殊特性之前,必须确定初始过程能力或性能的水平是可以接受的。 T
12、he level of initial process capability or performance shall be determined to be acceptable prior to submission for all Special Characteristics designated by the customer or supplier.,生产件批准程序 PPAP需编制的文件/项目,10.MSA result 量规測驗系統分析供方必须对所有新的或改进后的测量和试验设备进行适用的测量系统分析研究,如:量具的双性、偏倚、线性、稳定性研究。 The supplier shal
13、l have applicable Measurement System Analysis studies, e.g. gage R&R, bias, linearity, stability studies, for all equipment used for new or modified gages, measurement, and test equipment. 11.合格实验室文件化Approved Laboratory Documents供方必须具备实验室范围和文件 。 The supplier shall have a laboratory scope and documen
14、tation,生产件批准程序 PPAP需编制的文件/项目,12.控制计划 Control Plan供方必须具备规定用于过程控制的所有控制方法的控制计划。 The supplier shall have a Control Plan that defines all controls used for process control. 13.生产部件提交保证书 PSW warranty圆满完成了所有要求的测量和试验后,供方必须在零件提交保证书应填写保证书上所要求的内容。 Upon satisfactory completion of all required measurements and t
15、ests, the supplier shall record the required information on the Part Submission Warrant (PSW).,生产件批准程序 PPAP需编制的文件/项目,如果生产件是采用多腔铸模、工具、冲模或模型加工出来的,要求对由每一腔铸模等生产的零件进行完整的尺寸评价。 If production parts from more than one cavity, tools, die, pattern, or production process, e.g. line or cell, shall complete a dim
16、ensional evaluation on one part from each. 供方必须在保证书或附件中的特殊型腔/铸模/生产过程栏中注明提交的那些零件的特殊型腔和铸模等的编号。 The specific cavities, molds, line, etc., shall then be identified in the “Mold/Cavity/Production Process” line on a PSW, or in a PSW attachment. 证实了所有测量和试验结果符合顾客要求。 shall verify that all the measurement and
17、 test result show conformance with customer requirements,生产件批准程序 PPAP需编制的文件/项目,具备所有需要的文件(或者,对于等级2、3和4,在提交中已括) all required documentation is available (or, for Level 2,3, and 4, is included in the submission)供方负责人签署保证书并注明日期、职务和电话号码。 A responsible supplier official shall approve the PSW and provide da
18、te, title, and telephone number. 14.外观批准报告 (Appearance Approval Report)如果在设计记录上某一要求提交的零件或零件系列有外观要求,则必须完成该产品/零件一份单独的外观批准报告。 A separate Appearance Approval Report (AAR) shall be completed for each part or series of part for which a submission is required if the product/part has appearance requirements
19、 on the design record.,生产件批准程序 PPAP需编制的文件/项目,15.散装材料要求检查表 Bulk material requirement checklist对于散装材料,散装材料要求检查表必须经顾客和供方达成一致。For bulk material, the Bulk Material Requirements Checklist shall be jointly agreed upon by the customer and supplier. 16.顾客要求样品 Sample product as requested by customer供方必须按照顾客的要
20、求和提交要求的规定提供产品样品。 The supplier shall provide sample product as requested by the customer and as defined by the submission request.,生产件批准程序 PPAP需编制的文件/项目,17.标准样品由供应商保存Standard sample kept by supplier必须保存一件标准样品,与生产件批准记录保存的时间相同。 shall retain a master sample for the same period as the production part app
21、roval records 必须对标准样品进行标识,并在样品上标出顾客批准的日期。the master sample shall be identified as such, and shall show the customer approval date on the sample. 对于多腔冲模、铸模、工具或模型、或生产过程的每一个位置,除非顾客另有规定,否则供方必须各保留一件标准样品。 The supplier shall retain a master sample for each position of a multiple cavity die, mold, tool or p
22、attern, or production process unless otherwise specified by the customer.,生产件批准程序 PPAP需编制的文件/项目,18.使用的特殊辅助检具Special Aids- measurement equipments如果顾客提出要求,供方必须在提交PPAP时同时提交任何零件特殊装配辅具或部件检查辅具。 If requested by the customer, the supplier shall submit with the PPA submission any part-specific assembly or co
23、mponent checking aid. 19.顾客 特殊要求 Customer- Special requirements供方必须有与所有适用的顾客特殊要求相符合的记录。 The supplier shall have records of compliance to all applicable customer specific requirements.,要 求Requirement-1. 使用了有别以前批准过的零件的结构Use the parts that have different structure from the previous approved举 例 For exam
24、ple例如,在一个偏差(允差)上标明的或设计记录中作为注解包括进去的不同的加工方法,且又没有包含在工程更改中。Use the alternative working method as specified in the drawing, and without engineering authorization,通知顾客/顾客通知 Customer Notification,通知顾客/顾客通知 Customer Notification,要 求 Requirement-2使用了新的改变了的工具、模具、铸模、仿型Use new and changed tooling, mould, cavity
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