Chapter III- Section C of the AIAG MSA manual (3rd Edition) - Tired of analysis?

Atul Khandekar

Quite Involved in Discussions
#1
Chapter III- Section C of the AIAG MSA manual (3rd Edition) describes how a process team goes about conducting an Attribute Study using two methods. After some lengthy and tedious calculations the team gets two different results.

What surprised me was the paragraph after all this. On page 132, it says:

"Although these conclusions contradicted their previous results that there were no statistical differences among the appraisers, the team decided to go with these results since they were tired of all this analysis and these were at least justifiable since they found the table on the web."

What do you make of this? :confused:
 
Elsmar Forum Sponsor
M

M Greenaway

#2
Atul

It is very poorly worded isnt it. The explanation further down is a reasonable justification for the decision taken, i.e. the risk taken is up to the organisation, but the paragraph you quote does sound stupid to say the least.
 
Thread starter Similar threads Forum Replies Date
J Analysis of GRR studies, MSA 4th Ed, Chapter III section B - Rigid Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 1
K EU MDR Annex 1 Chapter III: Information in the Instructions for Use-23.4 (e) the performance characteristics of the device; EU Medical Device Regulations 1
V Preparing the IFU in compliance with MDR 745, Chapter III EU Medical Device Regulations 2
Rincewind MDR - GSPR - Annex I - Chapter II EU Medical Device Regulations 2
M MDR Annex IX Chapter I, 2.2 (c) - Device identification procedures during manufacture. EU Medical Device Regulations 1
C Access to Technical Documentation - MDR Chapter VI Article 61 EU Medical Device Regulations 4
L Connection between IEC 62304 and Chapter 14 of IEC 60601-1 IEC 60601 - Medical Electrical Equipment Safety Standards Series 2
Rameshwar25 Other types of Control Charts described in Chapter II of SPC Manual Statistical Analysis Tools, Techniques and SPC 6
W MDR Annex I chapter 23.2 (q) - Information required on the label EU Medical Device Regulations 17
N Sterility Testing - USP Chapter 71 and ISO 11737-2 ISO 13485:2016 - Medical Device Quality Management Systems 5
F ASQ chapter 1423 is now active in Lafayette ASQ - American Society for Quality 2
Ajit Basrur Detroit files for Chapter 9 bankruptcy amid staggering debts World News 4
L Temperature - IEC 61010-1 ed2 & ed3 at chapter 10 IEC 60601 - Medical Electrical Equipment Safety Standards Series 5
Hershal ASQ in China - Is there an ASQ Chapter in Shanghai? ASQ - American Society for Quality 2
Q Using Traceable Standards - AIAG MSA Manual Chapter II, Section B, 1st bullet Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 4
J Which chapter in Quality Manual will best fit this form (truck reservation)? Quality Management System (QMS) Manuals 1
S AIAG MSA (Measurement Systems Analysis) Manual 3rd ed. Chapter IV Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 6
O Numbers of units tested for Material/Performance Test - PPAP manual chapter 2.2.10.1 APQP and PPAP 1
J PMA Test and Computation Question - FAA order 8110.42C Chapter 2 section 6 b Federal Aviation Administration (FAA) Standards and Requirements 3
ccochran Planning & Implementing Solution (book chapter 5 on problem solving) The Reading Room 8
ccochran Identifying Causes (book chapter 4 on problem solving) The Reading Room 26
Marc GM Considering filing Chapter 11 Bankruptcy - 090216 World News 33
ccochran Understanding the Process (book chapter 3 on problem solving) The Reading Room 26
ScottK And people wonder why my ASQ chapter turnout is low... ASQ, ANAB, UKAS, IAF, IRCA, Exemplar Global and Related Organizations 12
T Confused by chapter numbering scheme in new standard (IEC EN-60601-2-37:2007) IEC 60601 - Medical Electrical Equipment Safety Standards Series 1
ccochran Selecting the Right Problem (book chapter 1) The Reading Room 8
ccochran Defining the Problem (book chapter) The Reading Room 26
Steve Prevette Red Beads in Ohio on May 21 - Kitty Hawk Chapter of the ASSE in Kettering Ohio ASQ - American Society for Quality 3
O Are you planning a 2nd Chapter? Career and Occupation Discussions 2
C Reducing Variation through Multiple Readings - MSA 3rd edition Chapter 5d Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 8
Jen Kirley Going to my local chapter's annual planning meeting ASQ, ANAB, UKAS, IAF, IRCA, Exemplar Global and Related Organizations 2
L A question of chapter 7 control chart of CQE BOK Professional Certifications and Degrees 1
C ISO 9001:2000 Chapter 7.2 - Problems to define product requirements ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 14
ccochran Chapter 2 of book - Your opinions please Book, Video, Blog and Web Site Reviews and Recommendations 5
ccochran Chapter 1 of book - Your opinions please Book, Video, Blog and Web Site Reviews and Recommendations 34
P MDR/IVDR Annex III - Technical documentation on PMS EU Medical Device Regulations 1
J Intervertebral body fusion cage, MDR Class II or Class III? EU Medical Device Regulations 4
A First CE-mark class III implantable device under MDD EU Medical Device Regulations 8
K Sterile barrier system symbols - Label redlines for a Class III device (Kit Box) EU Medical Device Regulations 0
K Class III Kit Box - Are translations mandatory under EU MDR? EU Medical Device Regulations 5
S Shipment of a CE Approved Class III Device to the EU Member States Other US Medical Device Regulations 1
C New Class III medical device application for Health Canada Canada Medical Device Regulations 6
M Changing supplier of critical raw material (III class device) Other Medical Device and Orthopedic Related Topics 1
B Class III Medical Device Accelerated conditions Other Medical Device Related Standards 1
E Different requirements for Class II and Class III Medical Devices Other ISO and International Standards and European Regulations 5
T Post-Market Surveillance Plan - Requirements outlined in Annex III (1.1b) EU Medical Device Regulations 2
Y Informational Change control process - Major vs Minor change - Active class III medical devices ISO 13485:2016 - Medical Device Quality Management Systems 12
A CE Mark PPE Category III for our customers residing in the EU CE Marking (Conformité Européene) / CB Scheme 1
A Class I medical device and Category III PPE - Long length gloves EU Medical Device Regulations 5
W CE Mark for Class III Medical Device - MDR or MDD applies? CE Marking (Conformité Européene) / CB Scheme 10

Similar threads

Top Bottom