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title 21
Food and Drugs
chapter I-i6
CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)
part 606
PART 606—CURRENT GOOD MANUFACTURING PRACTICE FOR BLOOD AND BLOOD COMPONENTS
subpart I
Subpart I—Records and Reports
Subpart 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.
