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.
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.
| 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 |
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| Export Percentage | 100% |
| Nearest Port | Guangdong, Shenzhen |
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