Dimensional measurement of components is routinely used throughout the Aerospace Industry to verify the conformance of the manufactured product to the specification. To ensure measurements are reliable, it is important to ensure the measurement capability is suitable for the feature being measured. Failure to implement and maintain effective measurement processes can lead to quality problems. It is therefore important for all aerospace manufacturers to operate effective measurement processes. There are a number of standards available that address Measurement & Inspection (M&I) issues, such as ASME Y14.5, ISO 17025, and ISO 10012. However, consistency of interpretation and application of these standards can be difficult, and existing customer or other party audits do not address the full scope to the level of detail required.
Consequently, the aerospace supply chain still experiences a number of issues related to measurement and inspection. The M&I Task group was established in 2012 to help address these industry concerns. Today, M&I conducts approximately 190 audits per year, and over 230 suppliers hold accreditation to M&I.
INDUSTRY SUPPORT
Participating Stakeholders:
B U S I N E S S B E N E F I T S
T E C H N I C A L B E N E F I T S
Reduction in nonconforming product by ensuring a more in-depth review of . . .
A U D I T C R I T E R I A
AC7130 – M&I Accreditation
AC7130/1 – Coordinate Measuring Machine
AC7130/2 – Laser Trackers
AC7130/3 – Articulating Arms
AC7130/4 – 3D Scanners
AC7130/5 – Mass Airflow Measurement of Turbine Engine Parts
AC7130/6 - General Inspection Tools
Mandates
Airbus, Airbus Defense and SAFRAN - AC7130/1/2/3
GE Aviation – AC7130/5
Rolls Royce – AC7130/4
C O M M O N I N D U S T R Y I S S U E S
COMMON NONCONFORMANCES FOUND DURING AN AUDIT
NCR 1
NCR 2
NCR 3
NCR 8
NCR 5
NCR 7
NCR 6
NCR 4
The Auditee provided evidence of a calibration certificate for the CMM (S/N #38, 3 Dec 2022), however the calibration results indicated “as-found, out of tolerance”. The Auditee could not provide evidence to indicate appropriate actions taken as result of the out of tolerance condition.
The Auditee could not provide evidence of an asset care process for the CMM equipment. The probe tip was contaminated with grease and dust and the guideways were covered with grit.
The Auditee could not provide records or any evidence of training, experience or on the job training (OJT) required for the Operators. The Auditee could not provide evidence of Operator approvals.
The Auditee could not provide evidence of current calibration for the CMM (PO records or calibration certificate). Calibration status was also not displayed on the CMM.
The Auditee could not provide evidence of flow-down of specific calibration requirements to the calibration source.
The Auditee could not provide evidence of a calibration certificate verification review when received from the calibration source.
The Auditee could not provide evidence that the Measurement System Software was verified to previous artifact data after two software updates and is in use.
The Auditee could not provide evidence of a process to manage the temperature around the CMM. During the audit, the ambient temperature was 6 degrees F above the industry standard.
NCR 9
The qualification sphere size indicated in the CMM software does not match the calibration size of the sphere listed on the calibration certificate.
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