From May 29, 2018 to May 31st, Wu Ke Long of the food and Drug Administration (KFDA) division of the Korean food and Drug Administration conducted a three day on-site audit in our company. The auditors carried out a careful and careful review of our company's hardware and software facilities. Through communication and communication with the production, quality, technology, procurement, human resources and other departments, the auditors fully affirmed that our company fully meets the basic requirements of the FDA certification regulations of the Korean government and the international standards of ISO.
The leaders of the company attach great importance to and require the relevant departments to pay close attention to them. According to the requirements of the audit, we should organize various departments to study together, and make suggestions for improvement on the shortcomings of human resources, calibration of measurement instruments and sterilization systems. QC, 5S management and ERP system management are compared with the original quality management system and find out their relationship. Contact and difference, make adequate preparation before audit. Every year, the company organizes relevant departments to study and publicize relevant quality systems.
This certification is conducive to the standardization of production management, to the improvement of the company's operation level and to the healthy development of the whole industry.
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