{"data":{"id":"us/10-cfr-35.7","jurisdiction":"us","citation":"10 CFR 35.7","heading":"FDA, other Federal, and State requirements.","body":"Nothing in this part relieves the licensee from complying with applicable FDA, other Federal, and State requirements governing radioactive drugs or devices.","path":["Title 10—Energy","CHAPTER I—NUCLEAR REGULATORY COMMISSION","PART 35—MEDICAL USE OF BYPRODUCT MATERIAL","Subpart A—General Information"],"source_url":"https://www.ecfr.gov/api/versioner/v1/full/2026-08-25/title-10.xml","current_through":"2026-08-25","vintage":"","retrieved_at":"2026-08-27T02:24:09Z","sha256":"18dbdd11d86be1d32a3e85df29653442f1d1c9dcf9521e603296669c9ac5357a","source_id":"us-cfr","stale":true,"prev":"us/10-cfr-35.6","next":"us/10-cfr-35.8"},"notice":"GroundRules: Original legal text. Not legal advice."}