SUBPART D—Importer Reporting Requirements (§803.40 to §803.42) - Title 21 - Food and Drugs CFR - USA Laws Searching

CFR > Title 21 - Food and Drugs > CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES > SUBCHAPTER H—MEDICAL DEVICES (parts 800 to 898) > PART 803—MEDICAL DEVICE REPORTING > SUBPART D—Importer Reporting Requirements (§803.40 to §803.42)

SUBPART D—Importer Reporting Requirements (§803.40 to §803.42)

803.40—If I am an importer, what kinds of individual adverse event reports must I submit, when must I submit them, and to whom must I submit them?
803.42—If I am an importer, what information must I submit in my individual adverse event reports?