[Federal Register Volume 72, Number 81 (Friday, April 27, 2007)]
[Notices]
[Pages 21031-21032]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 07-2085]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. 2007N-0068]


Medical Device User Fee and Modernization Act; Public Meeting; 
Correction

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice; correction.

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SUMMARY: The Food and Drug Administration is correcting a notice that 
appeared in the Federal Register of April 18, 2007 (72 FR 19528). The 
document announced a public meeting on April 30, 2007, to discuss the 
agency's proposed recommendations for the reauthorization of the 
Medical Device User Fee and Modernization Act of 2002 (MUDFMA I) for 
fiscal years 2008 through 2012, as well as other proposals to improve 
the review of medical devices and the third party

[[Page 21032]]

inspection program. The correction is being made to reflect a change in 
location for the April 30, 2007, meeting. The location of the meeting 
is being changed because of water damage in the original meeting 
location.

FOR FURTHER INFORMATION CONTACT: For information regarding this notice 
and the original notice, contact: Erik Mettler, Office of Policy and 
Planning, Food and Drug Administration (HF-11), 5600 Fishers Lane, 
Rockville, MD 20857, 301-827-3360, FAX 301-594-6777, email: 
[email protected]. For information regarding registration, 
contact: Cynthia Garris, Office of Communication, Education, and 
Radiation Programs, Center for Devices and Radiological Health, Food 
and Drug Administration (HFZ-220), 1350 Piccard Ave., Rockville, MD 
20850, 240-276-3150 ext. 121, FAX: 240-276-3151, email: 
[email protected].

SUPPLEMENTARY INFORMATION: In FR Doc. 07-1919, appearing on page 19528 
in the Federal Register of Wednesday, April 18, 2007, the following 
correction is made:
    1. On page 19528, in the third column, the first sentence under 
``ADDRESSES'' is corrected to read ``The public meeting will be held at 
the Food and Drug Administration, White Oak site, at 10903 New 
Hampshire Ave., Silver Spring, MD 20993, Bldg. 2, rm. 2031.''

    Dated: April 23, 2007.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. 07-2085 Filed 4-24-07; 3:18 pm]
BILLING CODE 4160-01-S