A full FAI report can include the part and lot identity, CAD or drawing revision, datum alignment, registration method, point-cloud or mesh coverage, color map, critical feature measurements, deviation statistics, tolerance results, calibration status, uncertainty, surface and final condition, reviewer, and disposition. The exact data set depends on the acceptance plan; a scan image alone is not a complete report. For an RFQ, provide the quantity, critical features, datum scheme, process route, post-processing state, file format, and delivery milestone.
Report Overview Section: The overview identifies the inspected configuration and the question the measurement is intended to answer. Record the material, process, part number, lot, drawing revision, measurement date, equipment, operator, and acceptance owner before reviewing the results.
Inspection Objective: Clear statement of analysis purpose (first-article validation, failure analysis, etc.)
Part Identification: Component name, drawing revision, serial number, and material specification
Executive Summary: High-level pass/fail determination with critical findings highlighted
Recommendations: Specific corrective actions or process adjustments
For critical applications in Aerospace and Aviation or Medical and Healthcare, the report should separate measured facts from engineering interpretation and identify any excluded feature, unresolved occlusion, or uncertainty. Aerospace or medical use requires project-level qualification; the report does not automatically establish airworthiness or biocompatibility.
Comprehensive Measurement Data: Measurement data should show nominal value, actual value, deviation, tolerance, units, datum or alignment basis, uncertainty, and pass, hold, or fail disposition. Include the feature list and analysis settings so a buyer can reproduce the review.
Actual vs. Nominal Dimensions: Tabulated comparison of all critical features with deviation values
Geometric Dimensioning & Tolerancing: Form, orientation, location, and runout per ASME Y14.5
Statistical Analysis: Cp/Cpk values for production batches and measurement uncertainty
Feature-Based Reporting: Organized by characteristic type (holes, planes, surfaces, etc.)
Powder Bed Fusion For a powder-bed build, relate surface deviations to build orientation, supports, process state, and final machining allowance where those fields affect interpretation. Verify critical dimensions after the final operation rather than transferring an as-built scan to the finished-part acceptance.
Metallographic Examination Results: Microstructure or surface observations can explain a geometric deviation, but they are separate evidence. If metallography, CT, or another inspection is included, link the sample, method, material lot, and final condition and record the limitation.
Grain Structure Analysis: Quantitative grain size measurements per ASTM E112 with distribution histograms
Porosity Quantification: Total porosity percentage, pore size distribution, and location mapping
Phase Identification: Microstructural constituents and their distribution
Defect Classification: Categorization and measurement of inclusions, cracks, and anomalies
This section is particularly critical for validating Heat Treatment processes and Hot Isostatic Pressing effectiveness on Titanium Alloy components.
3D Surface Characterization: A surface characterization section can report roughness or texture only when the scanner and analysis method support it. State the surface treatment, cleaning, resolution, uncertainty, and acceptance criterion; use a dedicated roughness or dimensional test when required.
Surface Roughness Parameters: Ra, Rz, Rq values with measurement locations indicated
Waviness Analysis: Longer-wavelength form errors from build process effects
Texture Direction: Lay pattern analysis relative to build orientation
Defect Mapping: Location and severity of surface anomalies
This data correlates directly with the effectiveness of subsequent Surface Treatment processes.
CT Scanning Data Interpretation: CT data may complement an optical scan for internal geometry, but the methods have different resolution, calibration, and uncertainty boundaries. Choose the additional inspection from the feature and acceptance question, then keep both reports linked to the same part and final state.
Volumetric Analysis: 3D visualization of internal features and defects
Wall Thickness Analysis: Color-coded maps showing thickness variations
Porosity Distribution: Location and size of internal voids with statistical summary
Assembly Verification: Clearance analysis and component fitment validation
Quality Conformance Assessment: The conformance conclusion should cite the drawing revision, tolerance rule, measured features, uncertainty, excluded areas, reviewer, and disposition. If evidence is incomplete, hold the part and request a remeasurement, CMM check, or approved deviation.
Material Specification Compliance: Verification against ASTM, AMS, or ISO standards
Process-Specific Requirements: Assessment against additive manufacturing guidelines
Customer Drawing Requirements: Feature-by-feature compliance status
Regulatory Compliance: FDA, FAA, or other industry-specific requirements
Comprehensive Visual Evidence:
Macro Photography: Overall part condition and identification markings
Microscopic Images: High-resolution micrographs at standardized magnifications (50X, 100X, 200X, 500X)
Scanning Electron Microscopy: High-magnification images for detailed fracture or feature analysis
Color-Coded Deviation Maps: 3D CAD comparison with deviation scales
Traceability Information: Traceability connects the scan to the supplier, material lot, build job, process revision, post-processing, equipment calibration, operator, and report version. Include those fields in the RFQ and verify the delivered record before release.
Inspection Equipment Details: Specific instruments used with calibration dates
Measurement Uncertainty: Stated uncertainty values for critical dimensions
Environmental Conditions: Temperature and humidity during measurement
Operator Information and Approval Signatures
Production Monitoring Metrics: Production monitoring can trend deviations by lot, machine, orientation, feature, and final condition. Use a defined alert limit and corrective-action rule, and do not confuse a trend signal with a confirmed nonconformance until the feature is verified.
Batch Analysis Trends: Historical data comparison for ongoing production
Statistical Summaries: Mean, standard deviation, and range for critical characteristics
Process Capability Indices: Cp, Cpk, Pp, Ppk values for qualified processes
Control Chart Data: For ongoing production monitoring
Quality Management Integration: Quality-system integration should define record retention, access, revision control, approval, and reinspection. The process is project-specific, so state who owns the acceptance decision and which data must be supplied with the part.
Risk Priority Numbers: For identified non-conformances
Root Cause Analysis: Initial investigation findings for failures
Corrective Action Requests: Formal documentation of required actions
Preventive Action Recommendations: Process improvements to avoid recurrence
Electronic Deliverables: Electronic deliverables should identify raw or processed data, file format, units, alignment, uncertainty, report revision, and any software requirement. Request the required package in the quotation, then confirm that every critical feature and disposition is present.
Raw Scan Data: Point clouds and mesh files in multiple formats
CAD Comparison Files: 3D models with embedded deviation data
Spreadsheet Data: Tabular results for further analysis
Custom Viewing Files: For proprietary analysis software
For Automotive component validation or Consumer Electronics first-article inspection, use a feature list, tolerance basis, surface state, and evidence depth matched to the acceptance standard. Record the release action instead of treating one report format as universal.