{"data":{"id":"us/21-cfr-58.202","jurisdiction":"us","citation":"21 CFR 58.202","heading":"Grounds for disqualification.","body":"The Commissioner may disqualify a testing facility upon finding all of the following:\n(a) The testing facility failed to comply with one or more of the regulations set forth in this part (or any other regulations regarding such facilities in this chapter);\n(b) The noncompliance adversely affected the validity of the nonclinical laboratory studies; and\n(c) Other lesser regulatory actions (e.g., warnings or rejection of individual studies) have not been or will probably not be adequate to achieve compliance with the good laboratory practice regulations.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER A—GENERAL","PART 58—GOOD LABORATORY PRACTICE FOR NONCLINICAL LABORATORY STUDIES","Subpart K—Disqualification of Testing Facilities"],"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":"f19f80ce6df37e8645e4616bf8aa4983bb0267cf1ca5d7436da118d59169026f","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-58.200","next":"us/21-cfr-58.204"},"notice":"GroundRules: Original legal text. Not legal advice."}