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GAO - 2009 FDA Medical Devices FDA Should Take Steps to Ensure That High-Risk Device Types Are Approved Through the Most Stringent Premarket Review Process

Apr 05, 2018

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    http://www.gao.gov/cgi-bin/getrpt?GAO-09-190http://www.gao.gov/cgi-bin/getrpt?GAO-09-190

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    http://www.gao.gov/cgi-bin/getrpt?GAO/PEMD-88-14

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    http://www.gao.gov/cgi-bin/getrpt?GAO-08-428T

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    http://www.gao.gov/

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    mailto:[email protected]

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    http://www.gao.gov/cgi-bin/getrpt?GAO-04-1022http://www.gao.gov/cgi-bin/getrpt?GAO-05-1042http://www.gao.gov/cgi-bin/getrpt?GAO-07-157http://www.gao.gov/cgi-bin/getrpt?GAO-07-996http://www.gao.gov/cgi-bin/getrpt?GAO-08-428Thttp://www.gao.gov/cgi-bin/getrpt?GAO-08-147http://www.gao.gov/cgi-bin/getrpt?GAO-08-780T

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    mailto:[email protected]:[email protected]:[email protected]://www.gao.gov/fraudnet/fraudnet.htmhttp://www.gao.gov/ordering.htmhttp://www.gao.gov/http://www.gao.gov/

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