Guidelines of Good Manufacture Practice (GMP)for Veterinary Drugs Manufacturers Article 41
The record of the returned product shall include the name, strength /contents, batch number, reason, quantity, treatment date and the final treatment method. The record shall be kept in compliance with the provision prescribed in Article 35.
中文原文 動物用藥品優良製造準則第41條
退回產品之紀錄應包括其名稱、含量、批號、退回理由、數量、處置日期及最終處置方式；其紀錄應依第三十五條規定保存之。