www.fdanews.com/articles/62525-actavis-announces-fda-warning-letter-following-fda-inspection
ACTAVIS ANNOUNCES FDA WARNING LETTER FOLLOWING FDA INSPECTION
September 14, 2006
Actavis Group, the international generic pharmaceuticals company, announced that it has received a warning letter from the U.S. Food and Drug Administration (FDA), related to its inspection of the Group's solid oral dose manufacturing facility in Little Falls, New Jersey.
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