The company once again passed the FDA inspection with zero defects
On March 23, 2017, the FDA inspector solemnly announced that Shandong Qifa Pharmaceutical Co., Ltd. will conduct a zero-defect on-site inspection! This is the 5th FDA inspection in the history of Qifa Pharmaceutical, and the 3rd time with zero defects.
This inspection involves material management, production management, quality management, laboratory management, packaging, and labeling systems. During the process, on-site and document inspections are interspersed, and high speed is required in terms of data provision. In the end, with the concerted efforts of various departments, the inspector was very satisfied with the operation of Qifa's quality system and spoke highly of the GMP operation of the entire company.
Qifa Company once again passed the FDA on-site inspection with zero defects, marking another big step towards becoming a technologically leading international enterprise.
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