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    APQP & PPAP Questionnaire

    Uploaded by

    Vilas

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    © All Rights Reserved
    Download as DOC, PDF, TXT or read online from Scribd

    APQP & PPAP Questionnaire

    Uploaded by

    Vilas
    6 views3 pages

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    Copyright:

    © All Rights Reserved
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    Download as doc, pdf, or txt
    6 views3 pages

    APQP & PPAP Questionnaire

    Uploaded by

    Vilas

    Copyright:

    © All Rights Reserved
    Download as DOC, PDF, TXT or read online from Scribd
    Download as doc, pdf, or txt
    of 3

    QUESSTIONNAIRE (BEFORE / AFTER)

    TOPIC : APQP & PPAP MARKS :

    DURATION : DATE :

    FACULTY : PARTICIPANT:

    (Tick the appropriate answer)


    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

    3. The no. of phases of APQP for manufacturers only


    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, inprocess & final
    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. spl. Characteristics
    c. critical characteristics

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


    a. 14
    b. 17
    c. 19
    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. Ppk > 1.67
    b. Cpk > 1.67
    c. Index value > 1.67
    14. Example of Chronically unstable processes is
    a. CNC turning
    b. Grinding process
    c. Grinding with auto dressing
    d. Moulding

    15. Cases for which customer interaction is required in initial process capability study is
    a. where enough data is not available (< 100)
    b. unstable processes
    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. laboratory scope & NABL Certificate & scope of certification for 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. 9
    c. 14
    d. 11

    18. Level 4 submission requires to


    a. retain all 19 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

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