SUBPART C—User Facility Reporting Requirements (§803.30 to §803.33) - 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 C—User Facility Reporting Requirements (§803.30 to §803.33)

SUBPART C—User Facility Reporting Requirements (§803.30 to §803.33)

803.30—If I am a user facility, what reporting requirements apply to me?
803.32—If I am a user facility, what information must I submit in my individual adverse event reports?
803.33—If I am a user facility, what must I include when I submit an annual report?