Medical Diagnostics / Diagnostic Center Corp. / Kentucky Memorial Hospital Inc. / Virginia Shenandoah Valley Mobile X-Ray Inc. / /
Country
United States / /
Currency
USD / / /
Event
Judicial Event / /
Facility
American College of Radiology / Port Royal Road Springfield / Memorial Dr. Manchester / Prisons facility / Fort Street Lincoln Park / Mary's Hospital / FDA facility ID / FDA Facility ID Facility / FDA Facility / /
IndustryTerm
mammography equipment / mammography web site / /
MedicalCondition
breast cancer / /
Movie
The Inspector General / /
MusicAlbum
Arkansas / Texas / /
Organization
State Board of Medicine / Division of Mammography Quality and Radiation Programs / FDA’s office of Health and Industry Programs / Food and Drug Administration / Bureau of Prisons / Health and Industry Programs Center for Devices / U.S. District Court / South Dakota office of Health Care Facilities Licensure and Certification Systems Development / FDA ACTIONS MQSA Actions Midwest Health Center / FDA’s office of Criminal Investigations / Mammography Quality and Radiation Programs office of Health / Medicare / Congress / federal government / National Cancer Institute’s Cancer Information Service / FDA’s office of Criminal Investigations Medical Diagnostics / Industry Programs Center for Devices / National Mammography Quality Assurance Advisory Committee / the American College / Michigan Midwest Health Center / National Technical Information Service / Cancer Information Service / M.S. Director Division of Mammography Quality / /
Person
Francis H. G. George / John L. McCrohan / Terry Alan Dichter / Patti Hoage / Gary Kaus / / /
Position
mammography technologist / government official / Inspector General / Governor / interpreting physician / Mammography Quality Advocate / radiologic technologist / MEDICAID ACTIONS The HHS Inspector General / /
Product
Phantom / /
ProvinceOrState
Texas / Kentucky / New Jersey / Virginia / Michigan / South Dakota / South / California / Iowa / Arkansas / /
May 15, 2003 Dear Mammography Quality Advocate: Under the Mammography Quality Standards Act (MQSA) of 1992, the Food and Drug Administration (FDA) is required to prepare and publish an annual report to assist health prof