SQP验厂审核内容有哪些

很多工厂一般会忽视一些细节问题，从而会导致验厂失败，停止订单的严重后果。下面通翔验厂认证一起来了解下有关SQP验厂审核对风险评估要求的相关知识。 ：

1、Quality Manual (including quality policy, objectives, organization chart, job description, reference to / procedures for the Quality Management System) 品质手册(包括质量方针，质量目标，组织架构图，工作职责描述，及与品质管理体系相关的程序)

2、 Internal audit documents (procedure, plan, audit report) 内审文件(程序文件，计划，评审报告)

3、 Management Review (procedure, agenda, report) 管理评审(程序，议题，报告)

4、 Supplier Control documents (supplier approval control procedure / criteria, list of approval supplier list, supplier evaluation records) 供应商管控文件(供应商评估控制程序/标准，合格供应商明细，供应商评估报告)

5、Inspection Specification / Instruction (including IQC, In-process, Final) 检验标准/指导(包括来料检验，制成检验及终检)

6、Work Instruction for each manufacturing process 作业指导：所有生产工序的指导

7、Document Control procedure (including that for record keeping) 文件控制程序(包括记录文件)

8、Procedure for definition and reporting of “incident” 事故定义及报告程序 9、Product recall procedure 产品招回程序

10、Corrective Action reports (related to incident, internal audit, complaint, etc) 改善措施报告(与事故，内审及投诉等相关的)

11、Test records on Traceability system 追溯体系的测试记录

12、Customer complaints procedure and complaint records 客户投诉程序及记录

13、Equipment maintenance documents (plan, procedure, record) 设备保养文件(保养计划，保养程序及保养记录)

14、Calibration of monitoring & measuring devices (plan, procedures, records) 监控及测量仪器的校验(计划，程序文件，记录)

15、Written procedure for handling glass and hard clear plastic breakages Cleaning schedule and procedure 书面玻璃及利器管控程序和清理安排

16、Pest control documents (list of trained pest control staff, contract with external pest control agency, pest control inspection record, bait documentation) 虫害控制文件(专业虫害控制人员名单，与外部虫害控制公司的合同书，虫害控制记录等)

17、Process flow documentation 工艺流程文件

18、Waste handling / storage procedure or record 废品控制/存储程序及记录

19、Record / plan for “Hazard Analysis” of the entire production processes 全部流程的风险评估计划及记录

20、Hazards Assessment records during product design and development 产品设计及开发过程中的风险评估记录

21、 Sharp tool control procedure & records (if applicable) 利器控制程序及记录(如果适用)

22、Nonconforming product control procedure 不良品控制程序

23、Guidance on quantity checking 产品数量检查指导

24、Approved reference samples 合格样品

25、Control procedure for equipment failure and process deviation 不良仪器的管控程序及隔离控制

26、Factory’s own training program (plan, procedure, records) 工厂内部的培训计划(计划，程序，记录)

27、Monitoring records of foreign body detectors (e.g. daily sensitivity records of metal detectors) 外来物品探测器(比如：每日金属探测记录)

28、Broken needle procedure & records (if applicable) 断针控制程序及记录(如果适用) 上述内容便是对的解答，大家对此应该有了一定的了解，如果您对此有什么疑问的话，可以点击在线咨询WWW.csr007.com或者电话进行详询，我们有专业的验厂咨询师与您交流作答。