e-CFR data is current as of March 4, 2021 |
Title 21 → Chapter I → Subchapter H → Part 822 → Subpart E → §822.24 |
Title 21: Food and Drugs
PART 822—POSTMARKET SURVEILLANCE
Subpart E—Responsibilities of Manufacturers
You must submit your plan to conduct postmarket surveillance to us within 30 days from receipt of the order (letter) notifying you that you are required to conduct postmarket surveillance of a device.