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BUREAU VERITAS India (IATF 16949 )

Examination for Internal Auditor Training Course for IATF 16949
EXAMINATION PAPER 2

Section 2 worth 10 marks

10 multi-choice questions from Core Tools (FMEA, MSA & SPC) which require you to place a
circle around the letter (a, b, c, d, e or f ) to indicate which you judge to be the best answer.
Each question is worth 1 mark. Answers may not be altered.

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1.01 APQP as per AIAG guideline aims on :

a Reducing / eliminating the quality problems

b Minimizing risk during product launch

c Timely completion of project

d all of the above

e none of the above.

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1.02 Total phases of APQP for a Non Design Responsible organisation

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a5

b4

c3

d May vary from product to product and organisation to organisation

e none of the above.

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1.03 Failure Mode and Effect Analysis requires

a Cross functional team approach

b Detailed knowledge of products / processes

c Prioritisation of action based on RPN

d a and b

e all of the above

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1.04 Manufacturing process design requirement of ISO/TS, needs to be

integrated

a with APQP at process design and development stage

b with APQP at Product Design and development stage

c a and b

d with APQP as appropriate.

e none of the above.

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1.05 FMEA is a tool for

a Prevention

b Correction

c Corrective action

d a and c

e all of the above.

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1.06 PFMEA should be consistent with

a The information in the process flow diagram

b Process flow diagram and shall be an input to Control Plan

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c All QMS documentation in manufacturing

d all of the above.

e none of the above.

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1.07 In case of DMEA

a Benchmarking studies, fail safe designs and error proofing is Prevention Control

b Design Reviews, Prototype testing, Validation testing and Reliability testing is Detection
control.

c Simulation of studies: as an analysis of concepts to establish design requirement is under

Prevention control whereas for validation of design it is detection controls

d all of the above.

e none of the above.

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1.08 In case of PFMEA

a Current controls to be consistent with the Control Methods specified in Control Plan

b Input comes from DFMEA and Process Flow Diagram

c Use of an RPN threshold is not a recommended practice.

d all of the above.

e none of the above.

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1.09 Control plan

a Must refer the control on all applicable product and process characteristics

b Must be referring reaction plan and corrective actions for each characteristics

c Must be implemented as per ISO/TS requirement

d all of the above.

e none of the above

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1.10 Control plan is one of the output of

a APQP

b MSA

c a and b

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