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Recalls and Alerts: July 31, 2012
date:Aug 01, 2012
ion Labs, Inc. (Reedsville, PA) that a December 2011/January 2012 inspection of the companys dietary supplement manufacturing facility revealed a failure to comply with the Current Good Manufacturing Practice (CGMP) regulations for Dietary Supplements.

FDA Warning Letter: FDA warns HL Jerch Sales, Inc., dba Bell Lifestyle Products, Inc. (South Haven, MI) that a February/March 2012 inspection of the companys dietary supplement labeling and distribution facility found significant violations of th

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