{"data":{"id":"us/21-cfr-1114.29","jurisdiction":"us","citation":"21 CFR 1114.29","heading":"FDA action on an application.","body":"After receipt of an application, FDA will:\n(a) Refuse to accept the application as described in § 1114.27(a);\n(b) Issue a letter administratively closing the application;\n(c) Issue a letter canceling the application if FDA finds that it mistakenly accepted the application or that the application was submitted in error;\n(d) Refuse to file the application as described in § 1114.27(b);\n(e) Issue a marketing granted order as described in § 1114.31; or\n(f) Issue a marketing denial order as described in § 1114.33.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER K—TOBACCO PRODUCTS","PART 1114—PREMARKET TOBACCO PRODUCT APPLICATIONS","Subpart C—FDA Review"],"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":"c1f8ae2054b56e860c6650898db491ee6d9a337835739235b85b9b0318818f6d","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-1114.27","next":"us/21-cfr-1114.31"},"notice":"GroundRules: Original legal text. Not legal advice."}