Federal Register Notice: FDA is correcting a notice that appeared in the 4/18 Federal Register announcing a public meeting on 4/30 to discuss the agency's proposed recommendations for the reauthorization of the Medical Device User Fee and Modernization Act of 2002. The location of the meeting is changed because of water damage in the original location; it is now FDA, White Oak site, at 10903 New Hampshire Ave., Silver Spring, MD 20993, Bldg. 2, Rm. 2031. To view this notice, click here.