R&D Center Manufacturing Center

Manufacturing Center

So far, SMISS has been equipped with the production hardware and environment of the industry's FDA standards. The supporting 7S management mode, GMP standard production environment, ISO9001 quality management system, and CNAS standard laboratory provide a guarantee for manufacturing and quality control. There are three modern automatic chemical plants covering an area of over 170,000 square meters; With a production team of over 10,000 people and a disposable e-cigarette production capacity of 100 million pieces, the company provides customers with a "one-stop service" integrating R&D, design and manufacturing.

  • 10000 +

    Workmates
  • 100 +million pcs/month

    Capacity
  • 170000 +

    Area
  • Production Scale

     

    3

    Large Production Base

    17K

    Production Area

    10000+people

    Number of Employees

    100million pcs/month

    Production of Atomizers

    50million pcs/month

    Production of Battery

    70million pcs/month

    Production of Disposable

    Core areas

     

    Production Environment
    Factory Standards
    Automation

    quality Management

     

    SMISS has been dedicated to quality improvement and has developed a unique proactive and preventive quality control model after years of practice. To ensure the delivery of quality products to customers, SMISS has developed stringent quality control systems and procedures. Every step from material procurement to finished product delivery, from workshop to laboratory, from staff to customers is reviewed to implement quality management, thus ensuring the maximum guarantee of product quality.


    The whole process of IQC (raw materials), IPQC (products) and FQC&OQC (finished products) follow strict quality control standards. Only after the product meets the specific standards of the production node can it proceed to the next step. The plants shall immediately modify or rework and file any nonconforming or defective products found in the inspection. The cause of nonconformance will be analyzed and a detailed corrective action plan will be developed to avoid the recurrence of the same problem.


    PFC

     

    IQC
    01
    LQC
    02
    FQC
    03
    OQC
    04