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판매
ISO 3951-1:2022
Sampling procedures for inspection by variables — Part 1: Specification for single sampling plans indexed by acceptance quality limit (AQL) for lot-by-lot inspection for a single quality characteristic and a single AQL- 발행일 : 2022-08-18
- 발행기관 : ISO
상세정보
분야 | ISO/TC 69/SC 5 : Acceptance sampling |
---|---|
적용범위 | This document specifies single sampling plans for lot-by-lot inspection under the following conditions: a) where the inspection procedure is applied to a continuing series of lots of discrete products, all supplied by one producer using one production process; b) where only a single quality characteristic, x, of these products is taken into consideration, which is measurable on a continuous scale; c) where production is under statistical control and the quality characteristic, x, is distributed according to a normal distribution or a close approximation to the normal distribution; d) where a contract or standard defines a lower specification limit, L, an upper specification limit, U, or both. An item is qualified as conforming if its measured quality characteristic, x, satisfies as appropriate one of the following inequalities: 1) x ≥ L (i.e. the lower specification limit is not violated); 2) x ≤ U (i.e. the upper specification limit is not violated); 3) x ≥ L and x ≤ U (i.e. neither the lower nor the upper specification limit is violated). Inequalities 1) and 2) are cases with a single specification limit, and 3) is a case with double specification limits. Where double specification limits apply, it is assumed in this document that conformity to both specification limits is equally important to the integrity of the product. In such cases, it is appropriate to apply a single AQL to the combined percentage of a product outside the two specification limits. This is referred to as combined control. |
국제분류(ICS)코드 | 03.120.30 : 통계적 방법의 응용 |
페이지수 | 107 |
Edition | 3 |
이력정보
No. | 표준번호 | 표준명 | 발행일 | 상태 |
---|---|---|---|---|
1 | ISO 3951-1:2022상세보기 | Sampling procedures for inspection by variables — Part 1: Specification for single sampling plans indexed by acceptance quality limit (AQL) for lot-by-lot inspection for a single quality characteristic and a single AQL | 2022-08-18 | 표준 |
2 | ISO 3951-1:2013상세보기 | Sampling procedures for inspection by variables — Part 1: Specification for single sampling plans indexed by acceptance quality limit (AQL) for lot-by-lot inspection for a single quality characteristic and a single AQL | 2013-08-27 | 구판 |
3 | ISO 3951-1:2005상세보기 | Sampling procedures for inspection by variables — Part 1: Specification for single sampling plans indexed by acceptance quality limit (AQL) for lot-by-lot inspection for a single quality characteristic and a single AQL | 2005-04-07 | 구판 |
관련상품
- ISO 3951-5:2006 - Sampling procedures for inspection by variables — Part 5: Sequential sampling plans indexed by acceptance quality limit (AQL) for inspection by variables (known standard deviation)
- ISO 3951-3:2007 - Sampling procedures for inspection by variables — Part 3: Double sampling schemes indexed by acceptance quality limit (AQL) for lot-by-lot inspection
- ISO 3951-4:2011 - Sampling procedures for inspection by variables — Part 4: Procedures for assessment of declared quality levels
- ISO 3951-2:2013 - Sampling procedures for inspection by variables — Part 2: General specification for single sampling plans indexed by acceptance quality limit (AQL) for lot-by-lot inspection of independent quality characteristics
- ISO 3951-6:2023 - Sampling procedures for inspection by variables — Part 6: Specification for single sampling plans for isolated lot inspection indexed by limiting quality (LQ)
다른 사람이 함께 구입한 상품
- KS Q ISO 3951-1 - 계량형 샘플링검사 절차 — 제1부: 단일 품질특성 및 단일 AQL에 대한 로트별 검사를 위한 합격품질한계(AQL) 지표형 1회 샘플링검사 규격
- ISO 11607-1:2019/Amd 1:2023 - Packaging for terminally sterilized medical devices — Part 1: Requirements for materials, sterile barrier systems and packaging systems — Amendment 1: Application of risk management
- ISO 5725-3:2023 - Accuracy (trueness and precision) of measurement methods and results — Part 3: Intermediate precision and alternative designs for collaborative studies
- ISO 11607-2:2019 - Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, sealing and assembly processes
- ISO 18113-1:2022 - In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions, and general requirements
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