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19 Mar 2018, 9:00 pm
Staff from the Food and Drug Administration inspected the Lake Charles, LA, location of Anna’s Pies LLC Jan. 9-11 and discovered “serious violations,” according to a March 9 warning letter made public by the FDA in recent days. [read post]
10 Sep 2010, 7:08 am
Food and Drug Administration will convene an expert advisory panel in September to determine whether to allow Meridia (sibutramine), a weight-loss pill produced by Abbott, to remain on the market. [read post]
3 Jul 2015, 7:11 am
The recall is a result of a routine sampling program by the Food and Drug Administration which revealed a “positive” test for Salmonella in Turkey Sprinkles. [read post]
13 Jun 2008, 10:40 pm
The chain's name and restaurant location are confidential, said David Acheson, the associate commissioner of foods for the Food and Drug Administration, during a conference call with reporters. [read post]
17 Jan 2017, 10:00 pm
“This recall was initiated with FDA inspection and sampling of the product,” according to the company’s recall notice posted on the Food and Drug ADministration’s website. [read post]
16 Nov 2019, 9:03 pm
Food and Drug Administration and co-chair of the online working group developing the revisions. [read post]
3 Mar 2024, 9:01 pm
As part of its enforcement activities, the Food and Drug Administration sends warning letters to entities under its jurisdiction. [read post]
25 Oct 2019, 9:36 am
Food and Drug Administration (“FDA”) and the Federal Trade Commission (“FTC”) issued a public statement regarding a joint warning letter sent to Rooted Apothecary, LLC, a Florida-based company, for unlawfully marketing several of its products containing cannabidiol (“CBD”). [read post]
25 Oct 2019, 9:36 am
Food and Drug Administration (“FDA”) and the Federal Trade Commission (“FTC”) issued a public statement regarding a joint warning letter sent to Rooted Apothecary, LLC, a Florida-based company, for unlawfully marketing several of its products containing cannabidiol (“CBD”). [read post]
29 Jan 2017, 10:00 pm
It isn’t long till the Food and Drug Administration is knocking on the door of the sprout supplier, telling company officials they have 24 hours to turn over a year’s worth of records for the outbreak investigation. [read post]
22 May 2022, 9:01 pm
As part of its enforcement activities, the Food and Drug Administration sends warning letters to entities under its jurisdiction. [read post]
23 Jun 2015, 10:01 pm
In his budget proposal for fiscal year 2016, President Obama proposed the consolidation of the Agriculture Department’s Food Safety and Inspection Service (FSIS) and the Food and Drug Administration’s food safety components into a new agency within the Department of Health and Human Services. [read post]
27 Jul 2012, 9:30 am
The plaintiffs argued that the generic drug manufacturers should be liable because the manufacturers 1) failed to warn about the risks associated with long-term use of the drug; 2) failed to request a labeling change revision with the United States Food and Drug Administration (FDA) as provided under the FDCA's "Changes Being Effected" provisions; and 3) failed to report safety information to the medical community. [read post]
22 Jan 2012, 5:42 pm
Food and Drug Administration said it also is conducting a data analysis but has not made any definitive conclusions and does not know when its review will be complete. [read post]
6 Mar 2018, 9:38 am
Plaintiff’s medical malpractice lawyer told the Herald there is no record the defendant nurse was tested by hospital administrators. [read post]
6 Mar 2018, 9:38 am
Plaintiff’s medical malpractice lawyer told the Herald there is no record the defendant nurse was tested by hospital administrators. [read post]
26 Dec 2012, 9:19 pm
Food and Drug Administration (FDA) are doing anything to replace MDP. [read post]
21 Feb 2017, 11:49 am
Food and Drug Administration (FDA). [read post]
26 Jan 2016, 11:23 am
Patent Nos. 8,007,826 (the '826 patent), 8,354,437 (the '437 patent), 8,440,703 (the '703 patent), and 8,663,685 (the '685 patent), have expiration dates from Jan. 18, 2025, to May 26, 2027, according to the Food and Drug Administration's Orange Book.Kyle Bass had petitioned for IPR review of the ‘685 patent and the ‘437 patents.See the IPBiz post The PTAB denial of the Bass IPR petitions on Acorda's Ampyra patents: not quite as… [read post]
29 Dec 2010, 5:37 pm
Recently, the Food and Drug Administration completed an investigation of 35% Food Grade Hydrogen Peroxide and Inositol and noted several FDA violations. [read post]