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商业 · 2011/7/71 分钟阅读
Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Draft Guidance for Industry, Third Parties and Food and Drug Administration Staff; Medical Device ISO 13485:2003 Voluntary Audit Report Submission Program
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摘要
The Food and Drug Administration (FDA) is announcing that a
来源原始语言: Federal Register — Health and Human Services打开原始公告 →