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Watchdog Verifies FDA Review Of Disputed Device Approvals

By Sindhu Sundar (October 8, 2015, 10:36 PM EDT) -- A key oversight office has accepted findings by the U.S. Food and Drug Administration's science and regulatory staff rejecting allegations by an anonymous whistleblower that the agency caved to special interests in approving certain diagnostic devices manufactured by General Electric and Carestream despite safety concerns....

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