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CFR 21
Food and Drugs
Food and Drug Administration, Department of Health and Human Services
Biologics
Current Good Manufacturing Practice for Blood and Blood Components
Records and Reports
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Section
606.160
Records.
Section
606.165
Distribution and receipt; procedures and records.
Section
606.170
Adverse reaction file.
Section
606.171
Reporting of product deviations by licensed manufacturers, unlicensed registered blood establishments, and transfusion services.