Controlled Drugs Act Article 33
The competent health authorities and the FDA may inspect and oversee the import, export, manufacture, selling, purchasing, administering, dispensing, and management of controlled drugs. Upon a showing of proper documentation the inspectors may sampling for testing. Said samples shall be limited to the amount of controlled drug needed for examination.
中文原文 管制藥品管理條例第33條
衛生主管機關及食品藥物署，必要時得派員稽核管制藥品之輸入、輸出、製造、販賣、購買、使用、調劑及管理情形，並得出具單據抽驗其藥品，受檢者不得規避、妨礙或拒絕。
但抽驗數量，以足供檢驗之用者為限。
但抽驗數量，以足供檢驗之用者為限。