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  1. LII
  2. Electronic Code of Federal Regulations (e-CFR)
  3. Title 21 - Food and Drugs
  4. CHAPTER I - FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
  5. SUBCHAPTER F - BIOLOGICS
  6. PART 606 - CURRENT GOOD MANUFACTURING PRACTICE FOR BLOOD AND BLOOD COMPONENTS
  7. Subpart I - Records and Reports

21 CFR Subpart I - Records and Reports

  • CFR
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  1. § 606.160 Records.
  2. § 606.165 Distribution and receipt; procedures and records.
  3. § 606.170 Adverse reaction file.
  4. § 606.171 Reporting of product deviations by licensed manufacturers, unlicensed registered blood establishments, and transfusion services.

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