
Quality Assurance Excellence
Achieve zero-defect manufacturing with advanced statistical process control and comprehensive testing protocols. ISO certified quality systems deliver <0.1% defect rates.
Comprehensive Quality Management
Zero-Defect Manufacturing Excellence
Our quality assurance program combines advanced statistical process control with comprehensive testing protocols to ensure every component meets the highest standards. With ISO 9001:2015, ISO 13485:2016, and IATF 16949:2016 certifications, we deliver consistent quality across all manufacturing processes. Our quality systems provide full traceability from raw materials to finished products, ensuring compliance with the most stringent industry requirements.

Key Highlights
- Advanced statistical process control (SPC)
- Real-time quality monitoring systems
- Comprehensive measurement and testing
- Full traceability and documentation
- ISO certified quality management
- Preventive quality approach
- Continuous improvement methodology
- Regulatory compliance expertise
Additional Capabilities

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Precision Measurement & Testing
Quality Control Capabilities
Our quality control capabilities encompass precision measurement, comprehensive testing, and advanced statistical analysis to ensure every component meets or exceeds specifications.
- Measurement Accuracy
- ±0.001mm
Precision coordinate measuring machine (CMM) capabilities for critical dimensions.
- Statistical Control
- Cpk >1.67
Process capability indices demonstrating statistical control and consistency.
- Defect Rate
- <0.1 PPM
Ultra-low defect rates achieved through preventive quality control measures.
- Testing Range
- Full Scope
Comprehensive mechanical, thermal, chemical, and dimensional testing capabilities.
Excellence Through Prevention
Quality Assurance Benefits
Our proactive quality approach prevents defects rather than detecting them, resulting in superior product quality, reduced costs, and enhanced customer satisfaction.
Zero-Defect Production
Achieve ultra-low defect rates through advanced statistical process control and prevention.
Cost Reduction
Eliminate waste and rework through first-time-right manufacturing processes.
Regulatory Compliance
Ensure compliance with all applicable industry standards and regulatory requirements.
Customer Confidence
Build customer trust through consistent quality and reliable performance.
Risk Mitigation
Identify and eliminate potential quality issues before they impact production.
Continuous Improvement
Ongoing process optimization based on quality data and trend analysis.
Precision Standards & Capabilities
Quality Control Specifications
Our quality control equipment and processes deliver industry-leading precision and reliability across all measurement and testing requirements.
Property | Value | Tolerance | Description |
---|---|---|---|
Gage R&R(% variation) Measurement SystemsProduction environment | ≤10% | Measurement System Analysis per AIAG MSA | |
Calibration Interval(months) CalibrationPer equipment class | 6-12 | ISO 17025 traceable equipment calibration schedule | |
Traceability Level(lot-to-serial) DocumentationAll regulated programs | Full | End-to-end material and process traceability | |
Critical Feature Inspection(coverage) InspectionPer drawing/CTQ list | 100% | Automated or manual inspection of CTQs | |
Sampling Standard(AQL) InspectionTypical AQL 0.65–1.0 | ANSI/ASQ Z1.4 | Attribute sampling per risk level | |
First Article Inspection(standard) QualificationPrior to serial release | AS9102 | Full dimensional layout and verification | |
PPAP Capability(levels) QualificationCustomer specified | Level I–IV | Automotive production part approval | |
CMM Uncertainty(mm) MetrologyMetrology lab conditions | ±0.001 | Accredited CMM verification per ISO 10360 | |
Vision Inspection Resolution(μm/pixel) Automated InspectionLighting-dependent | 5–20 | Automated optical inspection capability | |
Environmental Control(°C / %RH) EnvironmentMeasurement room | 20±1 / 45±5 | Temperature and humidity in metrology | |
Cleanroom Inspection(class) EnvironmentAs application requires | ISO 7/8 | Controlled environment for sensitive parts | |
SPC Sampling Rate(parts) Process ControlAdjustable by risk | Every 5 | Real-time control charting on CTQs | |
Nonconformance Response(hours) Corrective ActionsFrom notification | <24 | Immediate containment and 8D start | |
CAPA Closure(days) Corrective ActionsRisk-based | <30 | Root cause, actions, and verification | |
Record Retention(years) DocumentationContractual minimum | 10 | Traceability and quality records |