FDA Issues Details of the Dixie Dew Products Facility Shut Down
date:Apr 06, 2017
ew. On March 3, 2017, Dixie Dew refused to allow FDA investigators access to the facilitys environmental sampling and production records. So the FDA issued a Demand for Records under section 414 of the Federal Food, Drug, and Cosmetic Act. Dixie Dew then provided the government with the necessary records.

At the end of the inspection, FDA gave Dixie Dew a Form FDA 483, which is used when inspectors find objectionable conditions which may constitute violations of the Food Drug and Cosmetic (FDC)
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