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Biosan passed FDA on-site inspection with “Zero Deficiencies”
From May 22 to 23, 2025, the inspector of the U.S. Food and Drug Administration (FDA) conducted the on-site inspection on Zhejiang Biosan Biotech Co., Ltd. and gave the conclusion of "zero deficiencies" for the inspection.
The inspector conducted the inspection through on-site observation, random sampling, and employee interviews on various aspects of our company, including the workshops, facilities, technological processes, production records, testing methods & data, labeling, warehouses, factory environment as well as the quality management documents. The inspector concluded with a "zero deficiencies" result, and highly praised Biosan's managerial competence, team spirit, and employee ability.
It is the first time that we received the US FDA inspection. The excellent result of the inspection is derived from our unwavering commitment on the philosophy of that the quality is our life, our honesty and trustworthiness as well as making the excellence in every step of the process with the spirit of craftsmanship. Biosan will constantly enhance the self-capability and improve the management level to provide safe, effective, and high-quality mushroom products to customers around the world.
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