The FDA issued a warning letter to an Indian API manufacturer after inspectors found that the company knowingly accepted deliberately mislabeled raw materials to bypass licensing requirements, failed to perform required identity testing, and relied on unverified supplier documentation before using the materials to manufacture APIs shipped to the United States
Recalls & Warnings August 02, 2012 FDA Warns Two Supplement Makers of Manufacturing Violations On July 19, 2012, the FDA issued a warning letter to H & L Jerch Sales, Inc
Monisha, M., Suresh, A., Bapu, B
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