The Elsmar Cove Wiki More Free Files The Elsmar Cove Forums Discussion Thread Index Post Attachments Listing Failure Modes Services and Solutions to Problems Elsmar cove Forums Main Page Elsmar Cove Home Page
Welcome To The Old Cayman Cove Forums!
This thread is carried over and continued in the Current Elsmar Cove Forums


  The Old Elsmar Cove Forums
  QS-9000
  Setting FMEA Scope

Post New Topic  Post A Reply
profile | register | preferences | faq | search

UBBFriend: Email This Page to Someone! next newest topic | next oldest topic
Author Topic:   Setting FMEA Scope
Steven Sulkin
Forum Contributor

Posts: 75
From:Columbus, Ohio
Registered:

posted 04 August 1998 10:57 AM     Click Here to See the Profile for Steven Sulkin   Click Here to Email Steven Sulkin     Edit/Delete Message   Reply w/Quote
We are just starting FMEA's and I am trying to prevent infant mortality. I have two questions.

First Question
How narrow/broad to set the scope of FMEA's?

I have two concerns here. First, I dont want to manage 400 FMEA's. Second, I dont want the scope too narrow or broad to be of use. In your experience how should I set my scope?

To put a reference to this:
Scope 1: lense (too narrow?)
Scope 2: overhead projector (too broad?)

Second Question
How do you keep up your FMEA's? I am adding an FMEA review as part of the Corrective Action protocol (8-D), design review, and change board. It seems almost perenoid that every time we make a change we have to review FMEA's. Do most folks have a formal review schedule? Are the 8-D, Design review, and change board enough?

Thanks in advance.

IP: Logged

Marc Smith
Cheech Wizard

Posts: 4119
From:West Chester, OH, USA
Registered:

posted 05 August 1998 08:26 AM     Click Here to See the Profile for Marc Smith   Click Here to Email Marc Smith     Edit/Delete Message   Reply w/Quote
The scope of the FMEA is receiving to shipping. The level of detail is in line with your product and processes. There is no hard - fast rule regarding level of detail.I don't think 'Lens' is too small a detail - but, what about the lens? Wrong focal length? Clarity? These are things I would think about.

FMEAs are typically kept up by the product engineer or whoever 'plays' that functionary.

If you check out:

NC Database - Sample Record

You will see a place for FMEA and control plan review. As well as a print and other reviews. You make them part of the whole process. You review them and - if they need it - you update them. Typically there is going to be at least one problem during a year which would trigger a review of the documents.

On the other hand, as an auditor I would want to see that they are reviewed at least once yearly even if there are no problems. I don't think a yearly review is a requiment, though. I can't remember QS9000 stating a yearly review is required.

IP: Logged

All times are Eastern Standard Time (USA)

next newest topic | next oldest topic

Administrative Options: Close Topic | Archive/Move | Delete Topic
Post New Topic  Post A Reply
Hop to:

Contact Us | The Elsmar Cove Home Page

Your Input Into These Forums Is Appreciated! Thanks!


UBB 5.45c

Main Site Search
Y'All Come Back Now, Ya Hear?
Powered by FreeBSD!Made With A Mac!Powered by Apache!