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Rep. Syden "needlestick" investigation

This article was originally published in The Gray Sheet

Executive Summary

FDA submits response to a December inquiry by House Energy and COmmerce health subcommittee member Ron Wyden (D-Ore.) on FDA's regulation of needle-bearing devices ("The Gray Sheet" Dec. 21, I&W-8). A cover letter to the confidential document notes that FDA is helping the American Hospital Association to effect "a strategy for implementing the use of 'safer'needle-bearing devices in its member hospitals".
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