Information
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Program项目
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Document number文档编号
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Conducted on审核时间
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Auditor(s)审核人
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Audit participantor(s)审核参与人
Technical Information Availability有效技术信息
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Are actual drawings available at the lastest revision level?<br>实际图纸是否为最新修订版本?
Area setup区域设置
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Is the S.L.(Safe Launch)area properly identified?<br>安全量产区域是否被有效识别?
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Is there sufficient lighting?<br>工作台的灯光亮度是否足够?
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Is S.L.done in the cycle time?<br>安全量产是否在节拍时间内完成?
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Is the information posted?<br>信息是否张贴?
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Is there a designated rejection bin / rack and is properly identified?<br>是否有指定的不合格品箱并正确标识?<br>
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Does the area follow the 5S principles?<br>区域是否遵循了5S原则?
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Is there a process to ensure only certified parts are in the shipping container?<br>确保装运产品均为合格品?
Quality focus 质量关注
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Are S.L.Inspection instructions posted at the station?<br>检验作业指导书张贴在指定工位了吗?
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Is the S.L.inspection instruction approved?<br>作业指导书是受控的?
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Does the inspection criteria cover all features?<br>所有缺陷是否在作业指导书中明确?
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Special Characterisitics<br>特殊特性
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Is the S.L./quality gate an inspection gate?<br>是否有S.L?
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Are all gauges in good working condition?<br>是否所有检测量具处于良好的工作状态?
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Does the material flow follow the one piece principles?<br>检验产品遵循了单件流转?
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Is the flow of material through S.L.,and material status clearly identified?<br>物流是否通过S.L.,物料状态是否明确?
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Is there a reaction plan established and documented for all defects found in S.L.?<br>是否有针对所有缺陷的响应计划和文件在SL区域能找到?
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In case of a defect found at S.L. is there immediate feedback to the line?<br>SL区域发现不良是否马上返回至生产线?
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Are the S.L. Operators trained?<br>操作员是否培训过?
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Is there traceability to the operators that performed the S.L.?<br>产品标识可追溯性?
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Are there Master Samples available at the cell to confirm inspection?<br>有样件管理?在线样件放置?
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Does the S.L. gate verify all parts and components are packed and labelled properly?<br>所有产品被正确包装且标签正确?
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Is there a process to re-pack parts?<br>有重新打包的过程如返工产品跌落等?
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Is there a robust process in place to prevent shipment of material that has not gone through Safe Launch?<br>是否有有效的程序来防止发运的产品没有通过S.L.?
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Is S.L. done at the sub-supplier or component level?<br>分供方或零件生产过程中是否实施S.L.?
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Is there a process for documenting all S.L. findings?<br>是否有流程文件记录所有S.L发现的问题?
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Is there a process for tracking the S.L. findings?<br>是否有追踪S.L.发现的过程?
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S.L.findings review<br>S.L.结果审查
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Is there evidence of Management defective parts review?<br>是否有证据表明管理层对不良品的审查?
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Is there a process in place for documenting and tracking the problem reports from S.L./ quality gates?<br>是否有过程可以记录和跟踪来自S.L/ 质量门的问题报告?
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Are results of problem solving incorporated into quality documents?<br>问题解决的结果是否写入质量文件?
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If more that one shift is performing S.L./ Quality Gates checks,then does the part problem information pass across shifts?<br>如果有超过一个的班次,那么产品问题信息是否会传递到下一个班次?
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Exit Plan<br>退出计划
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Is there evidence of LPA by the plant leadership to verify S.L./ Quality Gate execution?<br>是否有工厂领导通过分层审核来验证S.l / 质量门执行的证据?
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Safe Launch Exit<br>结束
Sign-off 签名
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Signature
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Comments备注