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Question Whether FDA Knowingly Allowed Potentially Unsafe & Ineffective Drugs Into U. S. Market WASHINGTON, July 22, 2008 – Reps. John D. Dingell (D-MI), Chairman of the Committee on Energy and Commerce, and Bart Stupak (D-MI), Chairman of the Subcommittee on Oversight and Investigations, today launched an investigation into whether the Food and Drug Administration (FDA) knowingly allowed drugs suspected of being fraudulently approved and manufactured in gross violation of Good Manufacturing Practices (GMP) to continue being sold by Ranbaxy, Inc., in the United States. The investigation was prompted by information contained in a Motion to Enforce Subpoenas and Points and Authorities filed on July 3, 2008, with the U. day gambling cruises western fl idaho gambling online casino bonus 200 networking casino finance professionals act gambling and racin
