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Guidance for Industry, Third Parties and Food and Drug Administration Staff - Medical Device ISO 13485:2003 Voluntary Audit Repo

ICR 201412-0910-004 · OMB 0910-0700 · Object 52144601.

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Guidance for Industry, Third Parties and Food and Drug Administration Staff - Medical Device ISO 13485:2003 Voluntary Audit Repo
Corbin, Abigail
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2014-12-08
2026-10-13
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