FDA Acronyms and Abbreviations Database

Food and Drug Administration (FDA) conducts inspections of establishments that manufacture, process, pack, or hold FDA-regulated products, before approving products and/or after products are on the market, to determine the establishment’s compliance with the FDA laws. This document is called an FDA Form 483, which includes the name of the firm and the date(s) of inspection, and lists the observations made by the investigator during the inspection when there are objectionable conditions.

食品药品监督管理局（FDA）对生产、加工、包装或持有受FDA监管产品的机构进行审查，旨在在批准产品之前或产品上市之后，确认机构是否遵守FDA法律法规。该文件被称为FDA表格483，其中包含企业名称和审查日期，并列出审查员在审查过程中发现的任何令人不满的状况。