The Food and Drug Administration issued its weekly Enforcement Report for Nov. 14 that lists the status of recalls and field corrections for food, cosmetics, tobacco products, drugs, biologics and devices. The report covers both domestic and foreign firms.
On Nov. 14 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:
On Nov. 13 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:
On Nov. 9 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:
On Nov. 8 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:
On Nov. 7 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:
The Food and Drug Administration issued its weekly Enforcement Report for Nov. 7 that lists the status of recalls and field corrections for food, cosmetics, tobacco products, drugs, biologics and devices. The report covers both domestic and foreign firms.
On Nov. 6 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:
On Nov. 2 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:
The Food and Drug Administration on Nov. 5 issued a new guidance document outlining its mandatory recall authority under the Food Safety Modernization Act. The guidance includes a series of questions and answers on the basis for the relatively new authority, the process followed, what foods may be subject to mandatory recalls and how FDA determines whether a recall is necessary. Under FSMA, the “responsible party” for carrying out a mandatory recall is the food facility required to register with FDA that manufactured, processed, packed or held the food. FDA will give facilities a chance to conduct a voluntary recall before it exercises its mandatory recall authority, the agency said.