Regulatory Hearing Before the Food and Drug Administration

United States · Last verified: 2026-09-08

Number
21 CFR 16
Type
Regulation
Issuer
U.S. FDA
Status
in_force
Authority
FDA / CDRH

What this covers

FDA 监管听证程序:对行政扣留、强制召回令、禁用器械等行政行动提出并进行监管听证的启动、主持、记录、决定、复议与司法审查。

Official text: https://www.ecfr.gov/current/title-21/chapter-I/subchapter-A/part-16

Source: U.S. Food and Drug Administration (public domain)

Facts only; not legal advice. The official current text prevails.