The Food and Drug Administration issued its weekly Enforcement Report for April 22 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 April 20 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:
On April 17 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:
On April 10-15 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 April 15 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.
The Food and Drug Administration issued its weekly Enforcement Report for April 8 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 April 8 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:
On April 7 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:
On April 3 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 April 3 issued a new emergency use authorization (EUA) for importing non-NIOSH-approved N95 respirators from China, it said in a letter to importers, manufacturers and healthcare personnel. The EUA “makes KN95 respirators eligible for authorization if certain criteria are met, including evidence demonstrating that the respirator is authentic,” FDA said in a new frequently asked question added to its website. Chinese-made KN95 respirators had previously been ineligible for an EUA issued in late March for other non-NIOSH approved respirators “because of concerns about fraudulent products listed as KN95s,” FDA said.