FDA demands health documents from U.S. makers and importers



  • Executive summary
  • Introduction
  • The documents involved
  • Enforcement
  • Appendix 1: Definitions
  • Appendix 2: Necessary documents
  • Appendix 3: Document information

Product Description

Following the introduction this summer of the deeming regulations by the U.S. Food and Drug Administration (FDA), each vapour product manufacturer or importer is required to submit health documents describing the physiological, behavioural and toxicological effects of their tobacco products, current or future.

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