By: admin December 12, 2018 0 Comment.

$80 Million Fine Issued to Company for Failing to File Reports on Infections

\”Medical device adverse event reporting requirements are designed to protect Americans by providing FDA with a tool to detect potential safety issues. When device manufacturers fail to report adverse events, unsuspecting patients are placed at risk,\” said FDA Commissioner Dr. Scott Gottlieb, M.D.
Source: News feed

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