NS-ISO 2859-4:2002
计数抽样检验程序 第4部分:声明质量水平的评估程序

Sampling procedures for inspection by attributes - Part 4: Procedures for assessment of declared quality levels


 

 

非常抱歉,我们暂时无法提供预览,您可以试试: 免费下载 NS-ISO 2859-4:2002 前三页,或者稍后再访问。

您也可以尝试购买此标准,
点击右侧 “立即购买” 按钮开始采购(由第三方提供)。

 

标准号
NS-ISO 2859-4:2002
发布
2003年
发布单位
SCC
替代标准
NS-ISO 2859-4:2020
当前最新
NS-ISO 2859-4:2020
 
 
适用范围
  Full Description ADOPTED_FROM:ISO 2859-4:2002 This part of ISO 2859 establishes sampling plans and procedures that can be used to assess whether the quality level of an entity (lot, process, etc) conforms to a declared value. The sampling plans have been devised so as to obtain a risk of less than 5 % of contradicting a correct declared quality level. The risk is 10 % of failing to contradict an incorrect declared quality level which is related to the limiting quality ratio (see clause 4). Sampling plans are provided corresponding to three levels of discriminatory ability. In contrast to the procedures in the other parts of ISO 2859, the procedures in this part of ISO 2859 are not applicable to acceptance assessment of lots. Generally, the balancing of the risks of reaching incorrect conclusions in assessment procedures will differ from the balancing in the procedures for acceptance sampling. This part of ISO 2859 may be used for various forms of quality inspection in situations where objective evidence of conformity to some declared quality level is to be provided by means of inspection of a sample. The procedures are applicable to entities such as lots, process output, etc. that allow random samples of individual items to be taken from the entity. The sampling plans provided in this part of ISO 2859 are applicable, but not limited, to inspection of a variety of products such as — end items; — components and raw materials; — operations; — materials in process; — supplies in storage; — maintenance operations; — data or records; — administrative procedures. The procedures are primarily intended to be used when the quantity of interest is the number or fraction of nonconforming items for which the inspected items are classified as conforming or nonconforming. With minor changes, the procedures may also be used when the quantity of interest is the number of nonconformities or number of nonconformities per item. The necessary changes are: — replacement of “number of nonconforming items” by “number of nonconformities”; — replacement of “percent nonconforming items” by “nonconformities per 100 items”. In this case the values given in Tables 2 to 7 are only approximations.

NS-ISO 2859-4:2002相似标准


推荐

抽油杆拉力试验机引用标准主要有哪些

GB/T 191 包装储运图示标志GB/T 228.1-2010 金属材料 拉伸试验 1部分:室温试验方法GB/T 1220 不锈钢棒GB/T 1446 纤维增强塑料性能试验方法总则GB/T 1463 纤维增强塑料密度和相对密度试验方法GB/T 2828.1-2012 计数抽样检验程序 1部分:按接受质量(AQL)检索逐批检验抽样计划GB/T 3354 定向纤维增强塑料拉伸性能试验方法GB/T...

浅谈食品抽样检测方法

4.1计数检验方案与计量检验方案  4.1.1计数检验方案是指在检验产品质量时用计数方法,即判定批质量时只用到样本中不合格品数或缺陷数,而不管样本中各单位产品质量特性值如何。  4.1.2计量检验方案是指检验样本中每个单位产品质量特性值,并计算样本平均质量特性值来判定批质量水平抽样方案。  4.2抽样程序  按抽验程序分类可分一次、二次、多次以及序贯抽验等形式。  ...

检验产品检测报告具体应包含哪些信息?

一般检测报告应有以下信息:1)标题(例如检测报告、测试报告、检验证书、产品检验证书等)、编号、授权标识(CNAS/CMA等)和编号;2)实验室名称和地址,进行检测地点(如果与实验室地址不同);必要时给出实验室电话、电子邮箱、网站等;3)检测报告唯一性标识(如报告编号)和每一页上标识(报告编号+#页共#页),以确保能够识别该页是属于检测报告部分,以及表明检测报告结束清晰标识;4)客户...

实验室应该如何编制检测报告?

; 4)客户(委托方、受检方)名称和地址; 5)所用方法(含抽样检验和判定依据)识别(标准编号和名称); 6)检测物品描述、状态(产品新旧、生产日期等)和明确标识(编号); 7)对结果有效性和应用至关重要检测物品接收日期和进行检测日期; 8)如与结果有效性或应用相关时,实验室或其他机构所用抽样计划和程序说明; 9)检测结果,适用时,带有测量单位; 10)检测报告批准人姓名...





Copyright ©2007-2022 ANTPEDIA, All Rights Reserved
京ICP备07018254号 京公网安备1101085018 电信与信息服务业务经营许可证:京ICP证110310号