So we are a stamper. There are several stamping "processes" we lay out -- blanking, forming, piercing, trimming, etc. But not every part goes thru every one of those processes. So we cut them out and only include the relevant stamping steps. But some parts get plated or painted or other processes. For those we keep in the FMEA in order to match the boxes in our process flow, but just note that they are not applicable.
As per Ron's concern regarding subsequent changes, we treat every submitted (daughter) FMEA as "obsolete" when printed. The parent FMEA is kept up to date with changes. If we need a new one for a previous part, we just cut and paste again. We did this because managing 100s of FMEAs was unworkable and we couldn't keep up with revisions when something changed.
Hi Everyone,
I have a question regarding family PFMEAs. I'd like to put together a kind of modular FMEA system to cover all processes at the company like
- incoming material receiving
- internal transport
- warehousing
- melting
- casting/molding
- finishing
- machining
- etc.
- shipping
So my thoughts to have a matrix with all part numbers then group them into families and just make a matrix with marking which module applies to that family. The reason behind this is that the company has over 200 individual PFMEAs currently (in Excel, no software) and they are not maintained but the parts themselves sometimes very similar with minor differences. Processes also similar but of course the machining is creating different product characteristics for each individual product.
For the individual product characteristics, I plan to add a list of all important characteristics as one huge filterable spreadsheet as an appendix to the PFMEA.
PROS:
- approx. 15 modules PFMEA needs to be maintained in this way instead of the 200+ individual ones
- if I change something in the module that will apply to all PFMEA with uses the same module
- the review takes less time
CONS:
- for PPAPs, I need to put together the modules and save to my PPAP folder as the actual state in the time of submission (can be reviewed by customer on-site)
- hard to add the changes which only apply to one part specifically (e.g X part need higher melt temperature)
- problem with part characteristics
What are your thoughts? Can this work with IATF auditors/customer auditors?
Thank you in advance.
Hi Everyone,
I have a question regarding family PFMEAs. I'd like to put together a kind of modular FMEA system to cover all processes at the company like
- incoming material receiving
- internal transport
- warehousing
- melting
- casting/molding
- finishing
- machining
- etc.
- shipping
So my thoughts to have a matrix with all part numbers then group them into families and just make a matrix with marking which module applies to that family. The reason behind this is that the company has over 200 individual PFMEAs currently (in Excel, no software) and they are not maintained but the parts themselves sometimes very similar with minor differences. Processes also similar but of course the machining is creating different product characteristics for each individual product.
For the individual product characteristics, I plan to add a list of all important characteristics as one huge filterable spreadsheet as an appendix to the PFMEA.
PROS:
- approx. 15 modules PFMEA needs to be maintained in this way instead of the 200+ individual ones
- if I change something in the module that will apply to all PFMEA with uses the same module
- the review takes less time
CONS:
- for PPAPs, I need to put together the modules and save to my PPAP folder as the actual state in the time of submission (can be reviewed by customer on-site)
- hard to add the changes which only apply to one part specifically (e.g X part need higher melt temperature)
- problem with part characteristics
What are your thoughts? Can this work with IATF auditors/customer auditors?
Thank you in advance.
Hi Golfman25,
I know this post is over a year old, but it appears we are trying to implement the same changes that you went through. We also happen to be a metal stamping manufacturer as well so our processes are practically identical:
1) Receiving
2) Setup
3) Stamping
4) Cleaning
5) Outside service (clean, heat treat, and/or plating)
6) Final Inspection
7) Pack & ship
I really like your idea of having one controlled master PFMEA and Process Flow. Our thought was to do the same thing, but how do you address different Severity ratings for the same process? - for example an Inside Diameter may be a CC on one part and would therefore have a higher severity rating than the ID for other parts. Or a part may have several inside diameters, but only one of them is a CC. I have a hard time seeing how a Master PFMEA could capture all of those differences. I can send you a PM if you are willing to talk further. Thank you!!
Be creative and figure out what would work best for your situation. What doesn't work for us is 100s of PFMEAs floating around.
So we have a master FMEA. It contains every operation we do, i.e.; blank, trim, coin, draw, extrude, etc. Now every part does not see every operation. So to make a part specific FMEA we just delete everything that isn't relevant. We can then modify any of the numbers as we deem necessary, but that rarely happens. Now here is the key. Once it is printed, it is obsolete. We put it in the part file for reference purposes. But all future updates are done on the master. That way we catch the issues that can be applied across all parts. We sit down yearly and review the master, tweaking it as we see things come up over the years. Over the past 20+ years we have gone back and forth and back and forth and finally settled on this as it seems to work really well for us. I am sure by the book "FMEA gurus" would have issues with it, but it works for us.Thanks for the reply. I think the phrase "Perfect is the Enemy of Good" applies here. The Master/Family PFMEA's that we start developing won't be perfect, but it'll certainly be better than having 100s of PFMEAs.
That said though, I'm having a hard time picturing a PFMEA that you are describing with a "range" of ratings; or how you are "cutting and pasting" to create the daughter PFMEAs. Do you mean you have one (or several) Master PFMEAs with the generic process steps and a separate part-specific PFMEA that is just a skeleton with some miscellaneous "part-specific" ratings on it? When a part's PFMEA needs to be reviewed, then you temporarily copy the relevant steps from the Master PFMEA and paste it into the part-specific one?