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By: Chris Placitella @ Jan 09, 2013
St. Jude sends FDA letter regarding defibrillator leads. The Wall Street Journal (1/9, Weaver, Subscription Publication, 2.29M) reports St. Jude Medical Inc. sent a letter to Food and Drug Administration in which it admitted there were quality-control mistakes made during the development of its Durata defibrillator leads and provided details as to how it will […]
https://www.chrisplacitella.com/2013/01/09/product-safety-news/
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