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6 May 2010, 10:26 am
Food and Drug Administration: (FDA) McNeil Product Recall Information [read post]
6 May 2010, 9:43 am
The Food, Drug, and Cosmetic Act (“FDCA”) was enacted in 1938 to regulate, among other things, the drug and medical device industry in order to ensure the safe and effective design, manufacture, sale and labeling of such products. [read post]
6 May 2010, 2:59 am
Food and Drug Administration (FDA) have recommended that children under age six should not consume more than 6.0 micrograms of lead each day from all food sources. [read post]
6 May 2010, 2:59 am
Roughly 155,000 people work for local health departments across the United States. [read post]
5 May 2010, 12:08 pm
This authority is set forth in Section 518 of the Federal Food, Drug, and Cosmetic Act. [read post]
5 May 2010, 8:00 am
United States Attorney David Gaouette praised agents from the Food and Drug Administration Office of Criminal Investigations (FDA OCI) for their quick action, which led to Kay's arrest. [read post]
5 May 2010, 6:50 am
Prior to the incident, Medtronic, Inc. sought and obtained premarket approval from the Food and Drug Administration (FDA) to market this catheter as a Class III medical device under the MDA. [read post]
5 May 2010, 6:43 am
But the United States’ position, drafted by the Food and Drug Administration (FDA) and the Department of Agriculture (USDA), opposes this, stating that Codex should not “suggest or imply that GM/GE foods are in any way different from other foods” by allowing countries the option of mandatory labeling. [read post]
4 May 2010, 10:29 pm
The Food and Drug Administration (FDA) approved TOBI, an inhaled antibiotic, for the treatment of certain cystic fibrosis patients. [read post]
3 May 2010, 7:19 am
The Associated Press Saturday, May 1, 2010 WASHINGTON -- The Food and Drug Administration said Saturday it was investigating a health-care company for possible other problems following its recall of more than 40 over-the-counter infant's and children's liquid medications. [read post]
3 May 2010, 7:15 am
McNeil Consumer Healthcare, a division of Johnson & Johnson, voluntarily recalled the medications last Friday after the Food & Drug Administration (FDA) uncovered manufacturing deficiencies at the company's plant in Fort Washington, Pennsylvania. [read post]
3 May 2010, 6:05 am
Citing public safety concerns, the National Oceanic and Atmospheric Administration restricted fishing for at least 10 days in the affected waters, largely between Louisiana state waters at the mouth of the Mississippi River to waters off Pensacola Bay in Florida. [read post]
2 May 2010, 11:25 am
Food and Drug Administration to stop using these products. [read post]
2 May 2010, 8:26 am
Recently, the makers of Tylenol® (McNeil Consumer Healthcare, Division of McNEIL-PPC, Inc.) consulted with the Food and Drug Administration to voluntarily recall many over-the-counter children's and infants liquid products. [read post]
30 Apr 2010, 1:14 pm
Food and Drug Administration (FDA). [read post]
30 Apr 2010, 1:12 pm
Food and Drug Administration (FDA). [read post]
30 Apr 2010, 12:58 pm
Food and Drug Administration (FDA). [read post]
29 Apr 2010, 7:14 am
Initially, the drug was subject to warnings of these Avandia side effects after GlaxoSmithKline, the manufacturer of Avandia received prompting from the United States Food and Drug Administration (FDA). [read post]
28 Apr 2010, 11:49 pm
The United States alleges that Schwarz misrepresented the regulatory status of both drugs and failed to advise CMS that these unapproved drugs did not qualify for coverage under federal health care programs. [read post]
28 Apr 2010, 7:00 am
From January 1, 2001 through December 31, 2006, AstraZeneca promoted the sale and use of Seroquel for certain uses that the Food and Drug Administration (FDA) had not approved. [read post]
