Hi Lyfe Vaporz, LLC
Letter data
- Company
- Hi Lyfe Vaporz, LLC
- Recipient
- Jostin A Iriarte | Hi Lyfe Vaporz, LLC | United States | info@hilyfevaporz.com
- Issue date
- 2023-12-07
- Posted date
- Not available
- FDA office
- Center for Tobacco Products
- Subject
- Not available
- Product
- Tobacco
- CMS ID
- 614186
- Reference number
- RW2101567
- FEI
- Not available
- Inspection dates
- Not available
Normalized citations
21 CFR: 21-CFR-PART-114021-CFR-PART-1141
21 U.S.C.: 21-USC-301
Related FDA links
No related FDA letter link is present in the source index.
Full source text
CLOSEOUT LETTER
Hi Lyfe Vaporz, LLC
MARCS-CMS 614186 —
December 07, 2023
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Delivery Method:
VIA Electronic Mail
Reference #:
RW2101567
Product:
Tobacco
Recipient:
Recipient Name
Jostin A Iriarte
Hi Lyfe Vaporz, LLC
United States
info@hilyfevaporz.com
Issuing Office:
Center for Tobacco Products
United States
Secondary Issuing Offices
United States
Dear Jostin A Iriarte:
The United States Food and Drug Administration’s (FDA) Center for Tobacco Products (CTP) has completed evaluation of your corrective actions in response to FDA’s April 9, 2021 Warning Letter. Based on our evaluation, it appears that you have taken steps to address the violations contained in the Warning Letter. Future FDA inspections and regulatory activities will further assess the adequacy and sustainability of these corrections.
This letter does not relieve you or your firm from the responsibility of taking all necessary steps to ensure sustained compliance with the Federal Food, Drug, and Cosmetic Act (FD&C Act) and its implementing regulations or with other relevant legal authority. This letter also will not preclude any regulatory action should violations be observed in the future.
It is your responsibility to ensure that all of your tobacco products and all related labeling and/or advertising on any websites (including e-commerce, social networking, or search engine websites), in any other media in which you advertise, and in any retail establishments comply with each applicable provision of the FD&C Act and FDA’s implementing regulations. Failure to address any violations of the FD&C Act, 21 U.S.C. § 301 et seq., Chapter IX, relating to tobacco products including the tobacco regulations in 21 C.F.R. Parts 1140, 1141, and 1143, may lead to regulatory action, including, but not limited to, civil money penalties, seizure, and/or injunction.
If you have any questions, please contact CTPCompliance@fda.hhs.gov.
Sincerely,
/s/
Chad Burger
Director
Division of Product Compliance
Office of Compliance and Enforcement
Center for Tobacco Products
Content current as of:
09/13/2024
Regulated Product(s)
Tobacco