APA (7th ed.) Citation

United States. Government Accountability Office. (2009). Medical devices: FDA should take steps to ensure that high-risk device types are approved through the most stringent premarket review process : report to congressional addressees. U.S. Govt. Accountability Office.

Chicago Style (17th ed.) Citation

United States. Government Accountability Office. Medical Devices: FDA Should Take Steps to Ensure That High-risk Device Types Are Approved Through the Most Stringent Premarket Review Process : Report to Congressional Addressees. [Washington, D.C.]: U.S. Govt. Accountability Office, 2009.

MLA (9th ed.) Citation

United States. Government Accountability Office. Medical Devices: FDA Should Take Steps to Ensure That High-risk Device Types Are Approved Through the Most Stringent Premarket Review Process : Report to Congressional Addressees. U.S. Govt. Accountability Office, 2009.