21 CFR Part 803. November 4 ... and Reports on Devices) grants the FDA authority to require ... request from FDA for 5-day reports or identification of a ... http://www.gpo.gov/fdsys/pkg/FR-2014-02-14/pdf/2014-03279.pdf. 20 .... Medical-Device-Reporting21-CFR-Part-803 - View presentation ... Read free for days ... Medical Device Reporting 21 CFR Part 803: November 4, 2014 ... http://www.gpo.gov/fdsys/pkg/FR-2014-02-14/pdf/2014-03279.pdf. 20
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