Mammography Facilities, Standards, and Lay Summaries for Patients

United States Food and Drug Administration

Mammography Facilities, Standards, and Lay Summaries for Patients

OMB Control No. 0910-0309

No Material or Non-Substantive Change to a Currently Approved Collection (83-C)

FDA is requesting approval of a non-substantive change to form FDA 3422. This submission includes the new version of form FDA 3422 along with the redline version for comparison purposes. We are simply replacing all references to “FDA Mammography Quality Assurance Program” with “Mammography Quality Standards Act Program.”