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title 21
Food and Drugs
chapter I-i7
CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)
part 803
PART 803—MEDICAL DEVICE REPORTING
subpart D
Subpart D—Importer Reporting Requirements
Subpart D. Subpart D—Importer Reporting Requirements
§ 803.40 - If I am an importer, what reporting requirements apply to me?
§ 803.42 - If I am an importer, what information must I submit in my individual adverse event reports?
