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Regulations last checked for updates: May 14, 2025

Title 21 - Food and Drugs last revised: May 12, 2025
All TitlesTitle 21Chapter IPart 606Subpart I - Subpart I—Records and Reports
  • § 606.160 - Records.
  • § 606.165 - Distribution and receipt; procedures and records.
  • § 606.170 - Adverse reaction file.
  • § 606.171 - Reporting of product deviations by licensed manufacturers, unlicensed registered blood establishments, and transfusion services.
authority: 21 U.S.C. 321,331,351,352,355,360,360j,371,374; 42 U.S.C. 216,262,263a,264
source: 40 FR 53532, Nov. 18, 1975, unless otherwise noted.
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