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FDA Issues Warning to China API Maker

publication date: Mar 15, 2010
The FDA has told XiAn Libang Pharmaceuticals to improve its quality control procedures, if it wants to continue importing products to the US. The US agency told the company to hire an outside auditor to develop a Corrective Action Plan and respond to the warning letter within 15 days. According to the FDA, XiAn Libang did not conduct a thorough investigation after quality control problems were discovered last summer. More details...


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