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fda lawyer
(by tracywelsh) FDA requires facilities that manufacture, process, pack or store foods, drugs, and medical devices marketed in the U.S. file registrations with FDA. In addition, manufacturers of drugs and devices must list their products with FDA. These registrations and listings must be completed annually to stay in compliance with FDA regulations.
[Location: http://www.arrastia-law.com/practice-areas/international-trade/fda/]

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