FDA registration

關於「FDA registration」標籤，搜尋引擎有相關的訊息討論：

食品業者登錄平台 - 食品藥物管理署沒有這個頁面的資訊。

· 瞭解原因Search Registration and Listing | FDA2017年12月23日 · Releasable establishment registration and listing information under the Freedom of Information Act is available by searching the Establishment ... tw510(k) Premarket Notification - US Food and Drug Administration2018年1月26日 · Super Search Devices@FDA 6 ... MITAC INTERNATIONAL CORP. NO. 200, WEN HUA 2ND RD. GUISHAN DIST. taoyuan city, TW 33383 ...U.S. Food and Drug AdministrationThe FDA is responsible for protecting the public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, and ... twEstablishment Registration & Device Listing - US Food and Drug ...2. FDA Home3; Medical Devices4; Databases5. -. 1 result found for Establishment Registration or FEI Number : 3003559191 Owner Operator Number : 9050992 ...Documents Required Status | FDA2018年7月31日 · What documents should I provide to FDA? You should provide FDA with entry documentation which may include the following: Bill of Lading (BOL) ...Product Classification - US Food and Drug AdministrationResults 1 - 18 of 18 · powder-free polychloroprene patient examination gl ... Non-powdered patient examination glove. 880.6250, 1. OPH. radiation attenuating ...510(k) Clearances | FDA2021年6月9日 · Overview. Section 510(k) of the Food, Drug and Cosmetic Act requires device manufacturers who must register, to notify FDA of their intent to ... twRegistration and Listing | FDA2020年8月30日 · Domestic and foreign establishments that manufacture, repack, or re-label drug products in the United States are required to register with the FDA ... twWholesale Distributor and Third-Party Logistics Providers Reporting1-888-INFO-FDA (1-888-463-6332) Contact FDA · Subscribe to FDA RSS feeds Follow FDA on Twitter Follow FDA on Facebook View FDA videos on YouTube ...