Tagasi

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

Üldinfo
Kehtiv alates 18.08.2022
Direktiivid või määrused
puuduvad

Standardi ajalugu

Staatus
Kuupäev
Tüüp
Nimetus
18.08.2022
Põhitekst
27.08.2013
Põhitekst
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.
*
*
*
PDF
283,20 € koos KM-ga
Paber
283,20 € koos KM-ga
Standardi monitooring

Teised on ostnud veel

Põhitekst

EVS-EN ISO 14644-8:2022

Cleanrooms and associated controlled environments - Part 8: Assessment of air cleanliness by chemical concentration (ACC) (ISO 14644-8:2022)
Uusim versioon Kehtiv alates 15.07.2022
Põhitekst

EVS-EN ISO 10993-9:2021

Meditsiiniseadmete bioloogiline hindamine. Osa 9: Potentsiaalsete degradatsioonisaaduste tuvastamise ja koguselise kindlaksmääramise raamistik
Uusim versioon Kehtiv alates 15.10.2021
Põhitekst + muudatus

EVS-EN 62366-1:2015+A1:2020

Meditsiiniseadmed. Osa 1: Kasutatavusprojekteerimise rakendamine meditsiiniseadmetele
Uusim versioon Kehtiv alates 17.08.2020
Põhitekst

EVS-EN ISO 10993-1:2020

Meditsiiniseadmete bioloogiline hindamine. Osa 1: Hindamine ja katsetamine riskihaldusprotsessis
Uusim versioon Kehtiv alates 31.12.2020