WebFeb 27, 2024 · FDA Debarment List (Drug Product Applications) Below is a public list of firms or persons currently debarred pursuant to sections 306 (a) or (b) of the Federal Food, Drug, and Cosmetic Act (21 U.S ... WebInspection Classification Database Important Notes: Not all inspections are included in the database. Inspections conducted by States, pre-approval inspections, mammography …
FDA Dashboards - Compliance Dashboards - Food and Drug …
WebJun 29, 2024 · Warning LetterCMS # 613385. The U.S. Food and Drug Administration (FDA) inspected your drug manufacturing facility, Novel Laboratories, Inc. d.b.a. Lupin, FEI 3006271438, at 400 Campus Drive ... WebAug 29, 2012 · All Canadian drug establishments must hold, since January 1, 1998 an establishment licence to fabricate, package, label, distribute, import, wholesale, or test a drug. Guidance on veterinary antimicrobial sales reporting [2024-03-13] Management of Applications and Performance for Drug Establishment Licences (GUI-0127) Drug … bobcat ct2040
FDA Dashboards - Compliance Dashboards - Food and …
WebAug 19, 2024 · FDA issues export certificates for approved or licensed drugs and for unapproved drugs that meet certain legal requirements. FDA issues electronic certificates of pharmaceutical product (eCPP) for ... WebSearch criteria. You may search by either a) drug identification number ( DIN ), b) Anatomical Therapeutic Chemical ( ATC) code, or c) by company or one or more of the various other product characteristics listed. When typing inside fields, do not include punctuation marks such as hyphens, commas, colons, brackets and wildcard characters … Web7345.848: Inspection of Biological Drug Products Replaces 7342.006 - Inspection of Plasma Derivatives of Human Origin, 7345.001 - Inspection of Licensed Allergenic Products, 7345.002 - Inspection ... bobcat ct2035 backhoe