FDA this week released new draft guidance covering obligations when submitting cosmetic product facility registrations and product listings to the agency. The guidance outlines the various registration and product facility requirements for certain facilities, including import facilities, such as who is responsible for making the submissions, what information to include in the submissions, when to make the submissions and more.

On Aug. 4, FDA posted new and revised versions of the following Import Alerts on the detention without physical examination of:

On Aug. 3, FDA posted new and revised versions of the following Import Alerts on the detention without physical examination of:

On Aug. 2, FDA posted new and revised versions of the following Import Alerts on the detention without physical examination of:

FDA has issued its Enforcement Report for Aug. 2, listing 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 Aug. 1, FDA posted new and revised versions of the following Import Alerts on the detention without physical examination of:

On July 31, FDA posted new and revised versions of the following Import Alerts on the detention without physical examination of:

On July 27, FDA posted new and revised versions of the following Import Alerts on the detention without physical examination of:

On July 26, FDA posted new and revised versions of the following Import Alerts on the detention without physical examination of:

FDA will set the FY 2024 fee for its Voluntary Qualified Import Program at $14,975, it said in a notice. The fee, effective on Aug. 1, is up from $12,962 last year (see 2207270030) and is required from food importers and must be paid by Oct. 1 to begin participation in the VQIP trusted trader program for the period beginning Oct. 1, the agency said. The fee will remain in effect through Sept. 30, 2024, it said.