Manufacturing

Manufacturing

Freedom's FDA Registered (as a Tobacco Manufacturer), cGMP compliant automated facility in San Clemente, CA, U.S.A. has 6 custom engineered and fabricated machines, incorporating robotics, precision pneumatics and calibrated delivery pumps, we have the capacity to produce over 5 million units weekly right here in the United States of America.

  • Fully automated production assembly includes:
  • High speed e-liquid filling for cartridges and disposable e-cigarettes in an FDA Registered, dust free lab
  • Installation and wrap of custom outer product branding labels
  • Patent pending adhesive station for soft tip technology™ installation
  • Installation of finished air resistant silicone end caps

Our competitive pricing and quick turn-around times makes market entry fast and profitable.

Components Manufacturing

ISO 9001 Certified Facility
ISO 13485 Medical Device Certified
RoHS, CE, UL & FCC
GMP Certification

All components are manufactured to Freedom’s stringent standards

 

Manufacturing Components


Freedom’s U.S.-based Medical Device Manufacturer is ISO 13485:2003 certified. We produce our own proprietary patent pending soft filter tips.

The soft tips are fused to the PC disposable & cartomizer tubes, ensuring our products are safe, stay together, and deliver the most realistic smoking experience for the consumer.

 

Manufacturing Audits

Raw Goods
Work in Progress
Finished Goods
We certify samples with rigorous testing at each stage of the manufacturing process. This proven procedure ensures each component meets our high standards of quality.

Manufacturing Audits

Freedom conducts factory audits and personally visits with all sub-component suppliers: We ensure they maintain the highest standards including:

  • RoHS Compliance
  • QA Systems
  • Machinery Inspections
  • Work Flow
  • Cleanliness
  • Supply Chain
  • Management and Social Accountability

Audits

Automation Systems and QC

Our four custom-built automation systems – designed and made in America – are located in Southern
California. Freedom’s e-Liquids are made in ISO and GMP compliant labs in the United States.

Freedom’s U.S.-based Medical Device Manufacturer is ISO 13485:2003 certified. We produce our own proprietary patent pending soft filter tips.

We certify samples with rigorous testing at each stage of the manufacturing process. These proven procedures ensure each component meets our high standards of quality.

Automated QC is performed at multiple stages, any failed unit is rejected.

Automation System Includes:

  • Precision Filling
  • Gluing
  • Capping
  • Curing Tunnel
  • QC Inspection
  • Pressure Test
  • LED Light Test
  • Vapor Test
  • Labeling

Automated Process