Fda has different regulatory standards for different products: it requires fresh food safety; cosmetics are safe from poison; and medicines, medical devices, and biological and animal products are effectively safe. Food, health care and additives produced outside the united states are listed without the approval of the fda, provided that the fda is registered for clearance prior to listing. All offshore manufacturers (except cosmetics) are registered for production facilities and products prior to entering the united states market to allow fda to track and monitor the entire product. Among them, medicines and medical devices are the most strictly managed, which will review all laboratory results provided by the manufacturer and conduct on-site inspections of facilities。
