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Company Overview

An integrated corporation, VEG26 Vape Technology Co., Limited is specialized in the research, manufacturing, development, sales, and service of electronic cigarettes. The company boasts experts in both technology and management within its workforce.

The management philosophy of the company is centered around creating and offering the best and most innovative products to its customers. It adheres to the principle of putting customers first and relies on technological support as a cornerstone, providing clients with state - of - the - art technology and high - quality services.

VEG26 Vape products have been certified with CE, FCC, and ROHS. These items are marketed in the United States, Japan, Europe, and other regions across the globe. The company treats every customer with the highest level of care and consideration.

It believes that all tobacco users should have access to a greener and healthier alternative to traditional smoking.

An integrated corporation, VEG26 Vape Technology Co., Limited is specialized in the research, manufacturing, development, sales, and service of electronic cigarettes. The company boasts experts in both technology and management within its workforce.

The management philosophy of the company is centered around creating and offering the best and most innovative products to its customers. It adheres to the principle of putting customers first and relies on technological support as a cornerstone, providing clients with state - of - the - art technology and high - quality services.

VEG26 Vape products have been certified with CE, FCC, and ROHS. These items are marketed in the United States, Japan, Europe, and other regions across the globe. The company treats every customer with the highest level of care and consideration.

It believes that all tobacco users should have access to a greener and healthier alternative to traditional smoking.

 

Quality Control

COMPANY QUALITY CONTROL (QC) PROCESS

Ensuring Excellence at Every Stage

 

1. Purpose

To establish systematic procedures for monitoring, inspecting, and testing products/services against defined quality standards, ensuring consistent conformance to customer requirements, regulatory compliance, and company specifications.

 

2. Scope

Applies to all stages of production/delivery:

Incoming raw materials/components

In-process manufacturing/service execution

Final product/service verification

Post-delivery feedback analysis

 

3. Key Principles

Prevention Over Correction: Minimize defects through proactive controls.

Standardization: Follow documented procedures at all checkpoints.

Continuous Improvement: Use QC data to drive enhancements.

Accountability: Clear ownership of quality at each stage.

 

4. QC Process Workflow

Phase 1: Incoming Material Inspection

Activity: Verify supplier materials/components against specs (certifications, dimensions, functionality).

Tools: Checklists, sampling plans (e.g., ANSI/ASQ Z1.4), testing equipment.

Output: Accept/Reject/Quarantine decision; supplier non-conformance reports (if applicable).

 

Phase 2: In-Process Quality Checks

Activity: Real-time monitoring of critical parameters during production/service delivery.

Methods: Statistical Process Control (SPC), visual inspections, automated sensors.

Frequency: Defined per process risk (e.g., hourly/daily/per batch).

Output: Process adjustments, immediate defect containment.

 

Phase 3: Final Product/Service Verification

Activity: Comprehensive testing of finished goods/services against all requirements.

Tests: Performance, durability, safety, aesthetics, and functionality validations.

Documentation: QC test records, compliance certificates.

Decision: Release to market, rework, or rejection.

 

Phase 4: Audit & Calibration

Internal Audits: Monthly/quarterly reviews of QC adherence.

Equipment Calibration: Scheduled maintenance of measurement tools (traceable to standards).

 

5. Roles & Responsibilities

QC Technicians: Perform inspections/tests; document results.

Production Team: Execute in-process checks; escalate deviations.

QA Manager: Oversee process compliance; analyze QC data.

Suppliers: Provide certified materials; address non-conformities.

 

6. Handling Non-Conformities

Containment: Isolate non-compliant products/services immediately.

Root Cause Analysis: Investigate using 5 Whys/Fishbone diagrams.

Corrective Actions: Implement solutions (e.g., process adjustment, retraining).

Preventive Actions: Update procedures to avoid recurrence.

 

7. Records & Documentation

Maintain: Inspection logs, test reports, calibration records, non-conformance trackers.

Retention: All QC documents archived for [X] years (per regulatory/company policy).

 

8. Continuous Improvement

Data Review: Analyze QC metrics (defect rates, pass/fail trends) monthly.

Feedback Loop: Incorporate customer complaints/returns into QC refinements.

Process Updates: Revise QC checkpoints based on data-driven insights.

Certificates

品牌授权书

品牌授权书

Description

品牌授权书

品牌授权书

品牌授权书

Description

品牌授权书

品牌证书

品牌证书

Description

品牌授权书

品牌证书

品牌证书

Description

品牌授权书

品牌授权书

品牌授权书

Description

品牌授权书

Company Information

Business Type Supplier, Distributor/Wholesaler
Company VEG26 Vape Technology Co., Ltd
Main Products vape
Website https://www.vegvape.com/
Established Year 2018
City / State Croissy-Beaubourg , Île-de-France
Country/Region France
Address 3 ALLEE DU 1ER MAI

Factory Information

Location
Factory Size
Total QC Staff
Total RND Staff
Number of Production Lines
Annual output
Average Lead Time

Trading Information

Total Revenue
Export Percentage 100%
Nearest Port Guangdong, Shenzhen
Overseas Office
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