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United States Code
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Title 21 — Food and Drugs
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Chapter 9 — Federal Food, Drug, and Cosmetic Act
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Subchapter VII — General Authority
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Part H — Serious Adverse Event Reports
‹
Pt. G
Safety Reports
Pt. I
Reagan-Udall Foundation for the Food and Drug Administration
›
Part H — Serious Adverse Event Reports
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§379aa
Serious adverse event reporting for nonprescription drugs
§379aa–1
Serious adverse event reporting for dietary supplements
‹
Pt. G
Safety Reports
Pt. I
Reagan-Udall Foundation for the Food and Drug Administration
›
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