Recalls & Warnings
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Posted January 17, 2015
Maker of Magnesium and Potassium Supplements Warned for Manufacturing Violations
On December 23, 2014, the FDA issued a warning letter to Nutri Spec, Inc., following an inspection of facilities located in Pennsylvania and Indiana, which found the company's products, including A Good Thyme, Magnesium Chloride, Di-Potassium Phosphate, Sodium Citrate, Potassium Bicarbonate, Sodium Glycerophosphate, Potassium Citrate Electro Tonic, Oxygenic A-Plus, Oxygenic D-Plus and Phos Drops to be adulterated because they were prepared, packed, or held under conditions that violate Current Good Manufacturing Practices for dietary supplements.
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