Professional Documents
Culture Documents
Quality Control and Quality ASSURANCE (Contd.)
Quality Control and Quality ASSURANCE (Contd.)
Quality Control and Quality ASSURANCE (Contd.)
Chapter 28
SPC Errors
Type I error
Concluding a process is not in control when
it actually is or concluding that
nonrandomness is present when it is only
randomness that is present.
Type II error
Concluding a process is in control when it
is not that nonrandomness is not present
when it is present.
10-3 Quality Control
Type I Error
Figure 10.8
/2 /2
Mean
LCL
1 2 3 4
Sample number
10-5 Quality Control
(process mean is
shifting upward)
Sampling
Distribution
UCL
UCL
Does not
R-chart
LCL
detect shift
10-6 Quality Control
Sampling
Distribution (process variability is increasing)
UCL
Does not
x-Chart
LCL
reveal increase
UCL
Use of p-Charts
Use of c-Charts
Table 10.3
Use only when the number of occurrences per
unit of measure can be counted; non-
occurrences cannot be counted.
10-10 Quality Control
Run Tests
Trend
Cycles
Bias
Mean shift
Counting Runs
B A A B A B B B A A B
U U D U D U D U U D
10-14 Quality Control
Process Capability
Process variability relative to the specifications.
Tolerances or specifications
Range of acceptable values established by
engineering, design or customer requirements.
Process variability
Natural variability in a process.
Process capability
Process variability relative to specification.
10-15 Quality Control
Process Capability
Figure 10.15
Lower Upper
Specification Specification
A. Process variability
matches specifications
Lower Upper
Specification Specification
B. Process variability
Lower Upper
well within specifications Specification Specification
C. Process variability
exceeds specifications
10-16 Quality Control
Process Capability
Case C, A manager in case C can take the
following steps:
Redesign the process to obtain the desired output.
Use an alternative process to obtain the desired
output.
Retain the current process but attempt to eliminate
output using 100 percent inspection.
Examine the specifications to see if they are
necessary or can be relaxed.
10-17 Quality Control
Process Capability
Process Variability is the key factor in Process Capability.
It is measured in terms of process standard deviation.
Process capability is considered to be + 3 Standard
Deviations from the process mean.
An insurance company provides a service of registering a
new membership ( filling of form) in 10 mins, acceptable
range of variation around the time is + 1 minute, the
process has a standard deviation of 0.5min.It would not be
capable because + 3 SDs would be + 1.5 Mins, exceeding
the specification of + 1 minute.
10-18 Quality Control
specification width
Process capability ratio, Cp =
process width
1. Simplify
2. Standardize
3. Mistake-proof ( Poka Yoke)
4. Upgrade equipment
5. Automate
10-20 Quality Control
Traditional
cost function
Cost
Taguchi
cost function