美国食品药品监督管理局（US Food and Drug Administration，USFDA），成立于1906年，隶属于人类健康与卫生服务部，由国会（联邦政府）授权，是美国管理食品、药品以及化妆品等的主要行政监管部门、食品与药品监督管理的最高执法机关。 一、什么是FDA认证？ FDA是食品药品监督管理局（Food and Drug Administration）的简称，是由联邦政府授权，专门从事食品和 药品管理 的最高执法机关。 FDA认证旨在确保在美国市场上销售的产品符合FDA的安全性、有效性和质量标准。 The Food and Drug Administration (FDA) is a federal agency of the United States Department of Health and Human Services (HHS). 2026-06-30 115年度「檢驗方法線上投審稿系統功能擴充案」（案號：MOHW115-FDA-F-113-000717） 2026-05-08 115年度｢藥物、食品、化粧品優良實驗室管理資訊系統功能擴增案 (含維護)｣（案號：MOHW115-FDA-I-113-000723） Drugs@FDA includes most of the drug products approved since 1939. The majority of patient information, labels, approval letters, reviews, and other information are available for drug products approved since 1998. FDA Industry Systems (FIS) was created to facilitate making submissions to the U.S. Food and Drug Administration (FDA), including registrations, listings, and other notifications. The FDA is responsible for protecting the public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, and medical devices; and by ensuring the. The Food and Drug Administration (FDA) is responsible for protecting the public health by assuring the safety, efficacy, and security of human and veterinary drugs, biological products, medical devices, our nation's food supply, cosmetics, and products that emit radiation. The Data Dashboard contains data elements from FDA compliance and enforcement data sources, including Inspections, Compliance Actions, Recalls, Imports, and Food Safety Modernization Act programs. New dashboards with additional sources will continue to be added. The FDA has added bemotrizinol as an active ingredient for use in sunscreens, supporting greater consumer choice for safe and effective sun protection products.