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An FDA warning letter is an official message from the United States Food and Drug Administration (FDA) to a manufacturer or other organization that has violated some rule in a federally regulated activity. The FDA defines an FDA warning letter as:
Recently, many Wisconsin residents ― like people throughout the country ― have received letters warning of possible lead or unknown material in their water service pipes.
The letters are so called after Cyril Salmon, Baron Salmon, who first conceived of the idea in 1966 when chairing a report into how tribunals of inquiry were to be conducted. [ 2 ] The letters are also known as Maxwellisations after Robert Maxwell , who complained after criticism of his dealings in a public report. [ 3 ]
Tobacco package warning messages are warning messages that appear on the packaging of cigarettes and other tobacco products concerning their health effects. They have been implemented in an effort to enhance the public's awareness about the harmful effects of smoking. In general, warnings used in different countries try to emphasize the same ...
The FDA sent a warning letter Nov. 5 to parent company Colgate-Palmolive, which was publicly released Tuesday, detailing how microorganisms were found in water samples and finished toothpaste ...
(Reuters) -The U.S. health regulator has sent a warning letter to Cardinal Health after an inspection of its facility in Illinois found the company was marketing and distributing unapproved ...