• ISO 9001 Certified

Quality Control

CFS’s quality policy, “Customer First, Zero Defects,” promises a production pass rate of
99.8% and a product rework rate of less than 0.2%.

  • Six Sigma Management
  • Full-Process Coverage
  • Closed-Loop Management

99.8%

Production Pass Rate

<0.2%

Rework Rate

99%

Customer Satisfaction

100%

Traceability

Global Certifications & Standards

Our quality control system meets international safety standards and certifications

ISO 9001

Quality Management

UL Standards

2034 / 2075 / 217

European CE

EN 50291 / EN 14604

UKCA Marked

BSI Certified

Quality Control System

A comprehensive system spanning from incoming material control to outgoing quality assurance

Incoming Quality Control

IQC ensures all raw materials and key components meet specifications before production.

  • AVL vendor audits
  • AQL sampling standards
  • PPAP/COC verification
  • 8D analysis for non-conformance
In-Process Quality Control

IPQC monitors the entire production process to ensure consistency and stability.

  • First-article confirmation
  • SPC statistical control
  • 10% sampling inspection
  • Real-time anomaly handling
Outgoing Quality Assurance

OQA conducts final inspections to prevent non-conforming products from leaving.

  • AQL-based sampling
  • BOM compliance check
  • Function & appearance test
  • Complete traceability records

Incoming Inspection

All raw materials and key components are inspected according to PPAP, product specifications, or drawings

1
Vendor Verification

SQA checks if vendor is in AVL (Approved Vendor List)

  • Check vendor status upon MRN receipt
  • Hold unapproved vendor materials
  • Notify purchaser for resolution
2
Inspection & Sampling

Materials are inspected according to AQL standards

  • Inspection-exempt materials routed to stock
  • Appearance, dimension, and function inspection
  • AQL sampling standards applied
3
Non-Conformance Handling

8D analysis and MRB review for defective materials

  • Initiate 8D analysis for non-conforming materials
  • MRB review process
  • Record defective units for SPPM calculation
4
Release & Documentation

Quality Manager approval and documentation

  • Emergency releases require Quality Manager approval
  • Retain 10% samples for re-inspection
  • PPAP/COC verification before release
Key Control Points

Quality Manager approval and documentation

  • Materials must meet drawing specifications
  • Deviations result in return to supplier
  • Complete quality documentation required
  • Traceability from source to production

Note: Materials lacking PPAP or COC must be placed on “Hold” status until all quality and compliance documentation is complete.

Process Inspection Procedure

IPQC workflow ensuring product consistency through standardized documentation and multi-level inspection

Production Process Flow
1
Incoming Quality Control

Technical documents, equipment status, and personnel training must be completed and confirmed. Key processes identified with control plans.

2
First-Piece Inspection

Production line operator conducts first-piece inspection before mass production begins.

3
In-Process Control

Operators perform self-inspection and mutual inspection. PQA conducts patrol inspections following the process.

4
Anomaly Handling & SPC

Any abnormalities are reported immediately. Defective products are isolated, labeled, and managed for repair. Statistical quality control applied.

  • SPC Control

10% sampling with daily verification of production environment indicators (temperature, humidity, pressure).

  • Real-Time Monitoring

Immediate adjustment for any deviation to ensure stable production environment.

  • Continuous Improvement

Quality performance improved through data statistics and key issues analysis.

Outgoing Inspection Procedure

Ensuring finished products meet customer and regulatory requirements before delivery

1
BOM Verification

Check against Bill of Materials and engineering changes

2
Appearance Check

Visual inspection for cosmetic defects

3
Structure Test

Verify assembly and dimensional accuracy

4
Function Test

Validate all functional requirements

5
Packaging Check

Ensure proper packaging and labeling

6
Documentation

Complete traceability records

7
AQL Sampling

Statistical sampling based on Acceptable Quality Level

8
Release Approval

Final quality approval for shipment

Non-Conforming Batch Handling

For non-conforming batches, relevant departments implement defect control, root cause analysis, and corrective actions. This ensures only quality products reach our customers.

Reliability Testing

Reliability testing includes mechanical, electrical, and functional tests at the EP, PP, and MP stages, ensuring product stability and consistency
in real-world usage scenarios.This testing system is geared towards a 99% reliability target, effectively reducing the risk of
batch failures and enhancing product market adaptability and customer trust.
The list of reliability tests for the MP stage is as follows ⬇️

NO.

Test items

QTY

Apply to the model

Reference standard

Avoid Risk

1

LTC sensitivity test

32

PE, Photo Combo unit

UL217 42/UL268 31 EN14604 5.2/5.4 AS3786 5.3

Avoid the whole batch to false alarm or miss alarm

2

Heat sensitivity test

32

Heat Function Unit

UL521 19 UL539 14

Avoid the whole batch no alarm in high temperature environment

3

CO sensitivity test

32

unit with CO function

UL2034 41 EN50291 6.3.4

Avoid the whole batch no alarm or delaying alert at over CO concentration

4

Light output test

32

strobe light unit

UL1971 27

Avoid the whole batch insufficient visual alarms

5

Rate-of-Rise Operation Test

32

Heat Function Unit

UL521 23

Avoid the whole batch to miss detecting for the rapid temperature rise

6

Sensitivity Test Feature

5

ION, PE, ION/PE Combo unit

UL217 42.7 UL2034 43

False alarm or Missing alarm

7

Audibility test

32

All units with sound output

UL217 84/UL268 70 UL2034 65/UL539 23 EN14604 5.17 EN50291 6.3.16 AS3786 5.19

Avoid the whole batch lower 85dB at 3 meters

8

Alarm current (la). Standby current (Is) test

32

All units

CFS

Avoid the whole batch batteries lower lifespan

9

Static discharge test

5

All units

UL217 68/ UL2034 59 UL268 56 EN14604 5.14 AS3786 5 15b

Static electricity damages the chips

10

Low voltage (Battery) test

32

All units with battery

UL217 56.2 /UL268 45.2 UL2034 39.2 EN14604 5.16 EN50291 6.3.17 AS3786 5.17

Avoid the whole batch no alarm at the low batteries’ voltage

11

Abnormal operation test

32

All units

CFS

Avoid the whole batch software abnormal

  • 99% Reliability Target

Effectively reducing the risk of batch failures and enhancing product market adaptability.

  • International Standards

All tests adhere to UL217, EN14604, and UL2034 standards.

  • Lifecycle Testing

Testing at EP, PP, and MP stages ensures consistent quality throughout product lifecycle.

Traceability

Clear identification, complete data, and traceable processes covering the entire supply chain

Three Core Principles
1
Clear Identification

Unique identification through MRN, MO, P/N, serial number, and batch number

2
Complete Data

Inspection reports, production records, and transfer documents at each stage

3
Traceable Processes

Quick traceability to supplier, batch, and production line for anomalies

Process Coverage
Incoming Materials

SQA stage with MRN and inspection reports

Production

Work-in-process tracking with MO and batch numbers

Shipment

Final goods with complete traceability records

Note: All shipment products, finished goods, and semi-goods can be traced according to product name, P/N, D/C, PO, MO, and Lot No.

Customer Complaint Procedure

Comprehensive handling of customer quality issues with rapid response and 8D reporting

1

Immediate

Information Collection

Collect model, batch, quantity, and failure phenomenon

2

Within 1 business day

Temporary Measures

Implement measures to prevent problem escalation

3

Ongoing

Root Cause Analysis

Conduct RRCA to identify underlying causes

4

Within 10 business days

8D Report Submission

Complete 8D report with corrective actions

  • Performance Metrics

Customer satisfaction reached 99% over the past year, with no major complaints.

Applies to customer quality issue handling, recalls, field recall analysis, and COPQS collection.

Defective Products Control

Proper identification, isolation, and disposal of non-conforming products

Incoming Nonconformity
  • 8D analysis initiation
  • MRB review process
  • Supplier notification
  • Return or rework decision
Production Nonconformity
  • Immediate isolation and labeling
  • Root cause analysis
  • PDCA continuous improvement
  • Batch traceability
Outgoing Nonconformity
  • Hold shipment approval
  • Defect control implementation
  • Corrective actions
  • Re-inspection before release
Continuous Improvement

All defective products from the production line are recorded, and the quality and production departments analyze the causes, generate monthly reports, and issue corrective measures to continuously reduce the defect rate.

PDCA Cycle

Root Cause Analysis

Monthly Reports

Closed-Loop Management

Process of Incoming nonconformity
Process of Incoming nonconformity
Production process non-conforming
Production process non-conforming
Process of outgoing inspection nonconformity
Process of outgoing inspection nonconformity

Committed to Zero Defects

Our quality control system aims to prevent defective products from leaving the market, improve product stability,
and ensure product reliability in long-term operation.

  • Full-Process Coverage
  • Proactive Risk Management
  • Closed-Loop Management