FDA Guidance Documents·· 原文未提供具体时分
CPG Sec. 398.375 Obligations of Factory-based Manufacturers and Assemblers of Diagnostic X-ray Equipment Under the Performance Standard for Diagnostic X-ray Equipment
CPG Sec. 398.375 Obligations of Factory-based Manufacturers and Assemblers of Diagnostic X-ray Equipment Under the Performance Standard for Diagnostic X-ray Equipment
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FDA 官方历史目录记录；Final guidance；发布日期：1995-02-28。官方主题：Investigation & Enforcement, Radiology。请通过官方原文与附件查阅文件。
来源：FDA Guidance Documents · fda.gov