{"data":{"id":"us/21-cfr-10.200","jurisdiction":"us","citation":"21 CFR 10.200","heading":"Scope.","body":"This guideline describes FDA's policy and procedures applicable to electronic media coverage of agency public administrative proceedings. It is a guideline intended to clarify and explain FDA's policy on the presence and operation of electronic recording equipment at such proceedings and to assure uniform and consistent application of practices and procedures throughout the agency.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER A—GENERAL","PART 10—ADMINISTRATIVE PRACTICES AND PROCEDURES","Subpart C—Electronic Media Coverage of Public Administrative Proceedings; Guideline on Policy and Procedures"],"source_url":"https://www.ecfr.gov/api/versioner/v1/full/2026-08-25/title-21.xml","current_through":"2026-08-25","vintage":"","retrieved_at":"2026-08-27T02:24:47Z","sha256":"c9fd93ef25d210660407d32e577bf1f4e3484240e90b32c65194216ae37192d6","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-10.115","next":"us/21-cfr-10.203"},"notice":"GroundRules: Original legal text. Not legal advice."}