Information
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Audit Number
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Audit Title
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Department
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Workshop
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Conducted on
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Auditor/s
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Regulator/s
- EMAR
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Rating
- B1 - Engines
- B3 - APU
- C1 - Air Conditioning
- C2 - Autoflight
- C3 - Comms & Navigation
- C4 - Doors
- C5 - Electrical
- C6 - Equipment
- C7 - Engine - APU
- C8 - Flight Controls
- C9 - Fuel
- C12 - Hydraulic
- C13 - Instruments
- C14 - Landing Gear
- C15 - Oxygen
- C17 - Pneumatic
- C18 - Protection Ice/Rain/Fire
- C19 - Windows
- C20 - Structural Repairs
- D1 - NDT
- D5 - Arms, Munitions and Pyrotechnic Systems Specific
- other
Regulatory Approval
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AUDITORS NOTE: The checklist comments must contain sufficient information so that anyone reading it will clearly understand why the question received a compliant or non-compliant answer.
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Product Group
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1. Part Description
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2. Part Number
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3. Serial Number
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5. Is the product or process being audited included in (As applicable per NMAA being audited):
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EMAR 145 Certificate for Processes
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6. Is the facility where the product or process being audited included in:
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EMAR 145 MOE - 1.8
Process Approval
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7. Check the Work Package maintenance instructions are traceable back to the Customer Purchase Order and reflects the customer requirement i.e; Workscope, Modification/Service Bulletins etc.
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8. Is the work environment in compliance with the requirements detailed in the Component Maintenance Manual - CMM and suitable for the planned work.
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9. Is approved data (CMM, SPM, etc) available and current for the product or process being audited? Record CMM Chapter, Revision and Date.
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11. Preliminary Inspection & Hidden Damage Inspection
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a. Is a preliminary inspection conducted before work commences to identify damage?
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b. Is there a process to conduct a "Hidden Damage" inspection if the preliminary inspections identifies damage?
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12. Are there any Local Area Procedures (LAP's) applicable for the product or process being audited? If so, are they available and current.<br>Record LAP(s), Revision and Date.
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13. Ensure that tooling, fixtures and test equipment specified in the approved data are available, identified, controlled and where applicable the equipment displays a current calibration label.
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14. Check processes are in place for the approval of any alternate tooling being used in lieu of OEM specified tooling.
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15. Ensure that all calibrated tool used is within calibration.
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16. Ensure any 'Aids to Production' suitably identified and registered.
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17. Check part numbers of the parts replaced or software revisions align with the affectivity of the applicable approved data.
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18. Sample parts that are replaced and do traceability check to the originating Authorised Release Certificate or CofC (Standard parts).
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20. Check new parts and products packaging/storage requirements are being complied with, including any special storage requirements and shelf life control.
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21. Inspect any serviceable parts removed to ensure they are correctly stored and blanked to prevent damage and deterioration.
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22. Check specification materials detailed in the approved data are available with correct storage and shelf life controls. If alternate materials used check correct approval process are followed
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23. Check all the Parts, Materials and Consumable Products used during maintenance have been recorded
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24. Sample conformance with maintenance instructions i.e; Cleaning, Disassembly, Testing, Repairs Software revisions, Inspection criteria, NDT method/standard etc.
Certifying Staff
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25. Check the certifying staff is working within the scope of their maintenance authorisation verify staff awareness and access.
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26. Check that training records are available up to date and support the scope of the certifier’s authorisation.
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Check that staff are able to access relevant procedures
Certification of Maintenance
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27. Check completed stages of maintenance are supported with hard copy documentation including; NDT Reports, Tool to Task and Modifications etc.
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28. If Modifications have been implemented, have they been approved by the customer and have they been recorded on the Serviceable Label and ARC.
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30. (As applicable per NMAA being audited) Authorised Release Certificate completed correctly.
Packaging
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31. Is the Component correctly packaged for transport/storage as per the CMM.
Reporting
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32. Check the awareness of the defect reporting system
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33. Additional Information
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34. Record Findings for non compliances/observations and record numbers against the checklist item.