The Pharma Data
FEBRUARY 19, 2022
Food and Drug Administration is alerting the public that several categories of FDA-regulated products purchased from Jan. This alert covers FDA-regulated products purchased from Family Dollar stores in those six states from Jan. Today, the U.S. Families rely on stores like Family Dollar for products such as food and medicine.
The Pharma Data
MARCH 29, 2022
an animal food manufacturing company of Carney’s Point, New Jersey, has agreed to stop selling, manufacturing and distributing raw pet food and come into compliance with the Federal Food, Drug, and Cosmetic Act (FD&C Act). Food and Drug Administration (FDA) announced today that Bravo Packing, Inc., Related Information. Bravo Packing, Inc.
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XTalks
SEPTEMBER 17, 2020
The company has agreed to stop production until it takes remedial action and complies with the Federal Food, Drug, and Cosmetic Act. FDA Chief Counsel Stacy Amin said in a statement , “Manufacturing foods in violation of the Produce Safety Rule and Current Good Manufacturing Practice regulations places consumers’ health at risk.
FDA Law Blog
MAY 23, 2023
Specifically, field staff are advised to pay close attention to situations where allergen cross-contact may occur because of poor current good manufacturing practices (cGMPs), inadequate preventive controls, or inadequate controls under the juice or seafood HACCP regulations.
XTalks
JANUARY 18, 2021
CORE Network was created not only to manage foodborne illness outbreaks, but also to surveil and study post-response activities relating to illnesses linked to FDA-regulated food, supplements and cosmetics. coli contamination. coli outbreak. For example, in three years, there have been nine E.
The Pharma Data
SEPTEMBER 28, 2021
“The COVID-19 pandemic has accelerated the necessity for the FDA to assist make sure that foods ordered online and delivered on to consumers are safe to eat and not in danger of contamination. Food and Drug Administration will meet with members of the food industry, regulatory counterparts in the least levels of state , consumers, et al.
FDA Law Blog
JANUARY 1, 2024
Four of the letters addressed failure to comply with drug Current Good Manufacturing Practice regulations, four more stated that the recipients were distributing unapproved drug products, two alleged violations of the Quality System Regulation by medical device manufacturers, and one was addressed to a clinical investigator.
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