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    APQP+PPAP Questionnaire

    Uploaded by

    amit02mech
    The document is a 20 question multiple choice questionnaire about APQP (Advanced Product Quality Planning) and PPAP (Production Part Approval Process). Some key points covered include: - APQP stands for Advanced Product Quality Planning and involves 5 phases including process design and development where process FMEA is carried out. - Control plans should cover the process from receipt of materials to dispatch and PPAP has 3 submission levels. - Initial process studies for PPAP require a minimum trial run quantity of 300 consecutive parts and acceptance criteria of Cpk/Ppk greater than 1.67. - PPAP documentation includes 14 items and qualified laboratory documentation includes laboratory scope and certification of external labs.

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    © All Rights Reserved
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    APQP+PPAP Questionnaire

    Uploaded by

    amit02mech
    893 views3 pages
    The document is a 20 question multiple choice questionnaire about APQP (Advanced Product Quality Planning) and PPAP (Production Part Approval Process). Some key points covered include: - APQP stands for Advanced Product Quality Planning and involves 5 phases including process design and development where process FMEA is carried out. - Control plans should cover the process from receipt of materials to dispatch and PPAP has 3 submission levels. - Initial process studies for PPAP require a minimum trial run quantity of 300 consecutive parts and acceptance criteria of Cpk/Ppk greater than 1.67. - PPAP documentation includes 14 items and qualified laboratory documentation includes laboratory scope and certification of external labs.

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    The document is a 20 question multiple choice questionnaire about APQP (Advanced Product Quality Planning) and PPAP (Production Part Approval Process). Some key points covered include: - APQP stands for Advanced Product Quality Planning and involves 5 phases including process design and development where process FMEA is carried out. - Control plans should cover the process from receipt of materials to dispatch and PPAP has 3 submission levels. - Initial process studies for PPAP require a minimum trial run quantity of 300 consecutive parts and acceptance criteria of Cpk/Ppk greater than 1.67. - PPAP documentation includes 14 items and qualified laboratory documentation includes laboratory scope and certification of external labs.

    Copyright:

    © All Rights Reserved
    Download as PDF, TXT or read online from Scribd
    Download as pdf or txt
    893 views3 pages

    APQP+PPAP Questionnaire

    Uploaded by

    amit02mech
    The document is a 20 question multiple choice questionnaire about APQP (Advanced Product Quality Planning) and PPAP (Production Part Approval Process). Some key points covered include: - APQP stands for Advanced Product Quality Planning and involves 5 phases including process design and development where process FMEA is carried out. - Control plans should cover the process from receipt of materials to dispatch and PPAP has 3 submission levels. - Initial process studies for PPAP require a minimum trial run quantity of 300 consecutive parts and acceptance criteria of Cpk/Ppk greater than 1.67. - PPAP documentation includes 14 items and qualified laboratory documentation includes laboratory scope and certification of external labs.

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    © All Rights Reserved
    Download as PDF, TXT or read online from Scribd
    Download as pdf or txt
    You are on page 1of 3

    QUESSTIONNAIRE

    TOPIC : APQP & PPAP MARKS :

    DURATION : DATE :

    FACULTY : M C HARI PRAKASH PARTICIPANT:

    (Tick the appropriate answer) After


    Before

    1. APQP acronym means


    a. Appropriate product quality planning
    b. advanced product quality planning
    c. advanced techniques product quality planning

    2. Advanced product quality planning shall be carried out by


    a. MD/CEO
    b. MDT
    c. QAD
    d.
    3. The no. of phases of APQP are
    a. 3
    b. 5
    c. 2

    4. The phase during which process FMEA to be carried out


    a. product design & development
    b. product & process validation
    c. process design development

    5. The MSA & SPC are carried out during


    a. product design and development
    b. product & process validation
    c. process design development

    6. control plan to be prepared for


    a. prototype, prelaunch, production
    b. receipt only
    c. receipt, in process & final

    Page 1 of 3
    7. control plan should cover
    a. only receipt stage
    b. only final inspn. Stage
    c. from receipt to dispatch

    8. submission levels of PPAP


    a. 3
    b. 2
    c. 5

    9. Initial process studies to be carried out for


    a. All characteristics
    b. Special. Characteristics
    c. Quality characteristics

    10. No. of documents / items to be prepared for PPAP submission


    a. 14
    b. 17
    c. 18
    d. 11

    11. The weight in PSW form should be rounded off to


    a. 2 digits
    b. 3 digits
    c. 4 digits
    d. 5 digits

    12. Minimum trial run quantity during significant production run


    a. Min. 300 nos.
    b. min. 300 consecutive nos.
    c. min. 50 nos.
    d. 300 nos. in one shift

    13. Acceptance criteria for initial process study is


    a. Cpk / Ppk / Index Value > 1.67
    b. Cpk > 1.33
    c. Cp and Cpk > 1.0

    Page 2 of 3
    14. Example of Chronically unstable processes is
    a. CNC turning
    b. Grinding process
    c. Grinding with auto dressing
    d. Molding

    15. Cases for which customer interaction is required in initial process capability
    study is
    a. Where enough data is not available (<100)
    b. Unstable process
    c. Processes with one sided specification or non-normal data
    d. All of the above

    16. Qualified Laboratory documentation shall include


    a. laboratory scope
    b. In-house laboratory scope , NABL Certificate & scope of certification of
    external labs
    c. external Labs NABL certificate
    d. certificate of equivalent body

    17. The No. of situations for which notification & submission required is
    a. 8
    b. 12
    c. 14
    d. 11

    18. Level 4 submission requires to


    a. retain all 18 documents
    b. retain at app. Locations & submit to customer on request
    c. retain all docs. Only submit samples

    19. The appearance approval report is applicable for


    a. visual parameters
    b. visual attributes
    c. part has appearance requirements on the design record

    20. The part weight to be calculated using 10 parts from


    a. same cavity
    b. same tool
    c. same line
    d. each cavity, tool, line

    Page 3 of 3

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