Hi,
I have created a quality plant and assigned the MICs. When I am trying to Process the quality lot which is created automatically through QA32, I got an error, ,No inspection plan could be found'
When i create an inspection lot system is picking up the Task list and picking up the Sample size.
Please provide some light on this.
Hi Experts,
Requirement is Ststus change/Update via mobile access.
QM notification will have ststu profile with different statuses.
Example: Status Profile : QA Head Accept
QA Head Reject
On creation of Notification, alert should go to authorised user for the accept/Reject. user response should update back in SAP
Please throw some light on this configuration.
Which BAPI suffice this requirement.
Anyways Mobility team will do their configuration accordingly.
Thanks in advance
Hi Experts,
Iam trying to implement skip lot. Used DMR for lot creation.All are working fine but the Skipped lots cannot be made UD. All are in SKP status.
Tried using QA17 for making automatic UD but it is not working. Delay time made to 0 for testing purpose. Kindly advice your suggestion.
Regards,
VSR
Hi,
As soon as inspection lot gets created then email should go to specific user. We prepare inspection lot through qa01 and also when UD is been then automail should go to the concern person.
Please confirm how can we achieve this.
Regards,
Hi,
While doing the UD i am getting the message as you are not authorized. I have maintain the T-code in PFCG even then the error is coming.
Please find the screen shot of SU53 and also of PFCG
hi all-
I am going through and trying to figure a way to track User Status changes on the inspection lot. Does anyone know is there a user exit that allows us to turn enable the creation of change documents when change the status profile of inspection lots. It appears to be that the FM STATUS_CHANGE_EXTERN is called and has an option to record the change, but is not active in SAP native configuration/code. Anyway, I am looking now for a user exit off QA11 so we can record this, but if some one can help I would be grateful.
-Larry
Edited by: Rogers Larry on Jul 22, 2011 9:44 PM
=====================================
OK, all simplest approach is the best, the QM tab of the material master documentation required flag.
Hello Experts -Colleagues
I am in the kickoff stage of a new QM implementation.
Client has an established solution ECC 6.0, which does not have QM.
They are a regulated HACCP facility.
PP is installed. Process Orders drive inspection lot creation in other plants where QM was implements some time ago.
My question is:
Before I do any type of basic config., or development, what basic considerations should be thought through and planned out, prior to going forward. I'm aware of and have thoroughly read the QM prerequisites and building blocks.
My question is based on the fact that several settings for PP and SD are already in place which QM can and will negatively affect if not properly and carefully planned.
What type of basic checks should I make prior to any changes or config settings in my first sandbox and development clients??
This would be much easier if all modules were being implemented simultaneously as in a typical SAP launch including QM.
Hope the question is clear. I appreciate all help and different ideas. All answers are correct answers.
Sincerely,
Verroz
I am having a quality test of uniformity of content.
for this test we use 10 tablets as sample.
we analyse the each tablet for the active material content.
then we manually calculate the minimum, maximum, average and standard deviation.
I want to implement this in SAP.
I will put an MIC with sampling procedure with 10 sample size. So, the system will open 10 fields for result entry. this mic will not get printed. (Characteristics number 0010)
there will be other 4 mics with calculation formula for minimum, maximum, average and standard deviation. which will get printed on COA.
But, I don't know the formulas and where to put them in SAP. Please guide me to map the scenario.
Dipesh Bhavsar
Hi Guys,
I need a BADI/Exit for result recording process.
The process goes as follows..
I will go to QE51N TCODE then record result for MICs then close the results.When i come back again and put any MIC to in-process stage again then it should give me a pop-up to enter the reason for changing the recorded result.
Please give me the BADI/Exit name if you have worked on this requirement.
Hi Craig,
I have one query related to calculated characteristics
My requirement is to calculate Tensile Strenghth , my formula is as below
TS = Tensile Strength = Maximum load / ∏D2/4
How to define in formula in Inspection plan for specific formula.
Please help
Thanks & Regards,
Abhishek Patel
Hello Experts,
My Client business process requires Inprocess Quality check with stock posting.
I know the standard behaviour for 03 will not support for stock posting like Inspection type-04.
Is there any posiblity to do so..... (like BADI)
Kindly advise
Thanks,
Anand
Hi all
I have this problem and expect you can help me
1) I created a maintenance strategy whit the frecuencies 3, 6, 9, 12, 18, 24, 36, 48 and 60 months, We inclued all this frecuencies beacuse one material can have different studies with different duration
2) In CWBQM I selected all this packages (3,6,9,12,18,24,36,48,60)
3) In QST01 I created the stability study, with a scheduling period of 24 months.
When i Execute transaction IP30 the system creates:
one inspection lot for 3months frecuency
one inspection lot for 6months frecuency
one inspection lot for 9months frecuency
one inspection lot for 12months frecuency
one inspection lot for 18months frecuency
one inspection lot for 24months frecuency
one inspection lot for 36months frecuency
one inspection lot for 48months frecuency
The study duration in this case is 24 months, so I don't want aditional lots (36, 48 months)
I wonder if you could help me to identify why the system is having this behavior. I'd be glad to hear your opinion. Any ideas ?
diana
Hello All,
Is there any report which can show Quality Notification status open, and the usage decision for associated lot is complete?
Basically its compliance need to monitor lot UD is complete but associated notification is still in open status
Thanks
DD
Dear All.
We want to create QM order for Appraisal cost capture in every inspection lot for this we have done -
In material master Individual QM order is ticked for inspection type 01
Default order type QL02 is assigned to inspection type 01
1-Now requirement is we require creation of QM order automatically after GRN of PO means creation of inspection lot
2-Also same order we require to settle of Material master but while creation of QM order Manually in settlement receiver it's not allow to maintain the material master
Please suggest how can we do this
Regards
Dev123
Dear SAP'ians,
Hello,
Please help me to get rid over the below scenario ;
Please suggest the possible causes which may be responsible for it.
Thanks a lot.
Atul Mittal
I have one query related to calculated characteristics
My requirement is to calculate Tensile Strenghth , my formula is as below
TS = Tensile Strength = Maximum load / ∏D2/4
How to define in formula in Inspection plan for specific formula.
Please help
Thanks & Regards,
Abhishek Patel
Message was edited by: Craig S
Hi all
In one of my scenario i am facing issue related to confirmation of pooled sample.
As per standard procedure system always creates one physical sample (Category -Primary) automatically , pooled samples are created manually in reference to inspection lot.
Example:There are two primary samples 2.0 Kg each . These two samples unite to form a pooled sample of 4.0 Kg. Practically inspection only done for pooled sample. Hence there is no need to result record for primary samples.
I am attaching screen shots of sample drawing item.
I have already gone through SAP help and so many discussions , but not finding any proper explanation.
Regards
D Mohanty
Dear Gurus,
We have 3 quality labs and each lab is sent a separate samples to inspect certain characteristics once we receive material from production. I have created an inspection plan and mapped these three labs as work center in operation and then assigned MICs under each operation to inspect.
Now my issue is how to map separate 3 samples to inspection lot generated from production ( type-4) and also how to configure that to inspection plan.
I have to result record for all these three physical sample as withdrawn from Lot based upon inspection plan as mentioned above.
I can mention sample drawing procedure in inspection plan but how to map actual sample there.
Any help will be greatly appreciated.
Regards,
Satish
Hi all
Does anyone know if there is a BAPI to cover the functionality of these 2 transactions ?
I've had a look but haven't seen anything so far.
Many Thanks for any help
Alistair
Hi,
Is it possible restore a wrong deletion of a task list Group?
At moment, the task list Group'datas aren't archived and i can see it in PLAS and MAPL.
But when I execute QP02 i can't see the Group.
Thanks and best regards.
Antonio