Académique Documents
Professionnel Documents
Culture Documents
GUIDELINES/ CHECKPOINTS
APPLICABLE TOOLS
EVALUATION
Yes/No/NA Comments from Evaluator
2
3
GENERAL / PREPARATORY
Whether concern is logged into the centralized 'Concern Management System' (CMS) in server
and details periodically udapted therein?
Wherever concern is part related, whether supplier G8D is insisted upon?
Whether supplier G8D's are qualitatively evaluated as per this checklist?
Whether team has adequate understanding and knowledge of the overall G8D methodology?
For complex concerns requiring involvement from Field, PD, VD, Quality, SQA, mfg. etc, whether
----G8D's are initiated at multiple levels e.g. System level G8D; Part level G8D etc.?
1
2
3
a
b
c
e
f
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----------------Checksheet
Checksheet
----Checksheet / trend chart
Whether timelines for completion of each step for G8D clearly defined for tracking progress?
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1
2
3
4
5
6
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S.N.
GUIDELINES/ CHECKPOINTS
APPLICABLE TOOLS
EVALUATION
Yes/No/NA Comments from Evaluator
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b WHO? (Who is the person complaining? Write all the functions complaining about the problem.)
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WHERE? (a. Gegraphically the complaint is coming from. b. Where in the process flow and c.
Where in the component/ assembly?)
WHEN? (a. It first occurred? When all it has occurred? and when in product life cycle e.g. Kms,
d
days, hrs etc?
e HOW? (How did the person, identified in 'who' detect the problem?)
HOW BIG? (Quantify the problem in terms of a. Severity, b. Occurrence/ frequency, c. Value.
f
List down these 3 for every part number in 'what')
Whether photograph or skectch attached as appropriate for better clarity on the problem
2
statement?
Whether 'GOOD' & 'BAD' comparison is done through 'IS-IS NOT ANALYSIS' for the above 4W3
2H elements?
Whether actual place (GEMBA) visit made? And following details are checked?
4
A) Whether standards are present at suspected problem area?
B) Whether standards are known to the concerned persons and practiced?
Whether observations made during GEMBA is documented? And whether any conclusions
5
made?
Whether redefining the problem was needed based on the various observations (from past
6
data/Gemba observations)?
Whether details of D2 updated in the centralized 'Concern Management System' (CMS) in
7
server?
c
1b
2a
2b
3
4
5
6
Whether suspect material is segreggated, quarantined and tagged in the entire supply chain as
applicable (Field, warehouse, FG, EOL, In process, receipt stores, supplier and all transits)?
Whether details w.r.t. qty., cut off nos., implementation dates etc are captured properly
subsequent to above containment action?
Note : This is required when verification/ validation is mentioned as 'yes'.
Whether specific immediate actions are clearliy determined which may include additional
inspections/ checks, additional operations etc?
Whether details w.r.t. qty., cut off nos., implementation dates etc are captured properly
subsequent to above immediate action?
Note : This is required when verification/ validation is mentioned as 'yes'.
Whether documented & clear Work Instructions are provided for the above containment and
immediate actions so that there is no ambiguity while implementation & execution?
Whether the above is communicated through document or mail to all concerned and affected
parties?
Whether adequate supporting data is available & included in G8D report w.r.t. Effectiveness &
implementation of Interim actions (both containment & immediate actions)?
Whether % effectiveness of each action clearly identified based on fact and team consensus?
Checksheet
----Checksheet
SOP
----Checksheet / trend chart
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S.N.
GUIDELINES/ CHECKPOINTS
APPLICABLE TOOLS
EVALUATION
Yes/No/NA Comments from Evaluator
7
8
Whether other similar products/ processes identified where the above interim actions are
required to be horizontally deployed? If applicable, whether a plan for same is in place?
Whether details of D3 updated in the centralized 'Concern Management System' (CMS) in
server?
Note : Further steps should not stop after the interim action is taken and found that the
problem is not reported.
D4 - ROOT CAUSE VALIDATION
Whether brainstroming is adequately done to determine probable causes? Whether team of
process experts involved during brainstorming?
Whether causes are adequately addressed - whether cause definition is clear?
Whether C&E diagram prepared and primary secondary causes are adequately written?
Whether toosl like 'Difference-Change analysis' and 'Change timeline' used for arriving at
probalble causes?
Are causes further stratified in terms of :
- Escape cause
- Occurrence cause
- System cause
a. Whether there is clear justification for coming from probable to root causes?
b. Whether past data of D0 & D3 (stratified data) is used for identifying probable causes?
Whether adequate data is collected for identified probable causes?
Whether data collected is analyzed systematically using various data based tools as applicable?
9
10
11
1
2
3
4
12
13
2
3
4
5
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Brainstorming
Brainstorming
C&E diagram
Difference change analysis,
change timeline
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- Graphs/Charts/Stratification/
Stratified pareto/Control Charts/
Histogram/Scatter plots/DOE/
Data based decision
- Other validation tools as
applicable
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Brainstorming
Tree diagram/ Decision making
worksheet/ Solution selection
matrix
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S.N.
GUIDELINES/ CHECKPOINTS
APPLICABLE TOOLS
EVALUATION
Yes/No/NA Comments from Evaluator
1
2
3
4
5
6
7
8
9
10
11
12
13
----------------Checksheet
SOP
----Checksheet / trend chart
--------Checksheet / trend chart
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1
2
3
4
5
Whether standards for new methods are prepared? Revising the existing standards :Drawings,
specifications, DFMEA, DVP, PFD, PFMEA, Control Plan, SOP, Checklists etc?
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Date opened:
D0 - Problem Defination
Last updated on:
Product/Process Information:
D0 Symptom(s):
% Effective
No. of
vehicles
Field
SPD
Yard
Plant (Post CAI)
Others
Remarks
Date Implemented
Member
Title
Location
Phone
Date opened:
Last updated on:
m meeting frequency :
meeting held on :
e-mail