Ansi Asq Z1 4 2003

Posted on by

American Society for Quality. ANSI/ASQ Z1.4-Foreword. Iii (This foreword is not a part of the American National. Standard— Sampling Procedures and Tables for Inspection. By Attributes, Z1.4-2003) This standard is a revision of ANSI/ASQC Z1.4-1993, “Sampling Procedures and Tables for Inspection. Attributes.” Beyond editorial refinements. – Notice 1 cancelled the standard and refers DoD users to ANSI/ASQC Z1.4-1993. ANSI/ASQ Z1.4 – Current version is ANSI/ASQ Z1.4: 2008. FDA Recognition – The FDA recognizes ANSI/ASQ Z1.4-2008 as a General consensus standard – Extent of Recognition: Use of all Single, Double and Multiple sampling plans. For a complete explanation of AQL see: The Importer's Guide to Managing Product Quality with AQL C D E E F G S4 A A B C G H C SINGLE SAMPLING PLAN FOR NORMAL INSPECTION, ANSI/ASQ STANDARD Z1.4-2003. Presented on April 25, 2017AbstractAcceptance sampling is a common method to determine if the output of a process, the product, should move to the next proce.

AnsiAnsi
-

Z1.4–2003 would like to confirm if ASQ Z1. It is a business andi for you to make if your customer is not demanding it. My question is about sampling aluminium foils, films used in packaging and sticker labels received in rolls which are wound around a core. What is the difference between ANSI/ASQC Z1.4 1993 and ANSI/ASQ Z1.4-2003?

510(k)|DeNovo|Registration & Listing|Adverse Events|Recalls|PMA|HDE|Classification|Standards
CFR Title 21|Radiation-Emitting Products|X-Ray Assembler|Medsun Reports|CLIA|TPLC
Ansi/asq z1.4-2003 (r2013) standard

Ansi Asq Z1 4 2003 R2018


Ansi/asq Z1.4-2003

Asq

Ansi/asq Z1.4-2008

New SearchBack To Search Results
Part B: Supplementary Information Sheet (SIS)
038Date of Entry01/27/2015
Standard
ANSI ASQZ1.4-2003 (R2018)
Sampling Procedures and Tables for Inspection by Attributes
Scope/Abstract
This publication establishes sampling plans and procedures for inspection by attributes. When specified by the responsible authority, this publication shall be referenced in the specification, contract, inspection instructions, or other documents and the provisions set forth herein shall govern. The 'responsible authority' shall be designated in one of the above documents, as agreed to by the purchaser and seller or producer and user.
Extent of Recognition
Complete standard
Rationale for Recognition
This standard is relevant to medical devices and is recognized on its scientific and technical merit and/or because it supports existing regulatory policies.
Public Law, CFR Citation(s) and Procode(s)*
Regulation NumberDevice NameDevice ClassProduct Code
§884.5300Condom§884.5300Condom, Synthetic§884.5310Condom With Nonoxynol-9§878.4460Surgeon'S Gloves§880.6250Latex Patient Examination Glove§880.6250Patient Examination Glove§880.6250Polymer Patient Examination Glove§880.6250Vinyl Patient Examination GloveFDA Technical Contact
William MacFarland
FDA/OC/CDRH/OPEQ/OHTII/
301-796-5547
william.macfarland@fda.hhs.gov
Standards Development Organizations
American National Standards InstituteASQhttps://asq.org/
FDA Specialty Task Group (STG)
General I (QS/RM)
*These are provided as examples and others may be applicable.