Session Supply Company
Letter data
- Company
- Session Supply Company
- Recipient
- Dutch Knudson | Session Supply Company | United States | dutch@sessionsupply.com
- Issue date
- 2021-06-08
- Posted date
- Not available
- FDA office
- Center for Tobacco Products
- Subject
- Not available
- Product
- Tobacco
- CMS ID
- 612797
- Reference number
- RW2101470
- FEI
- Not available
- Inspection dates
- Not available
Normalized citations
21 CFR: None found
21 U.S.C.: None found
Related FDA links
No related FDA letter link is present in the source index.
Full source text
CLOSEOUT LETTER
Session Supply Company
MARCS-CMS 612797 —
June 08, 2021
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Delivery Method:
VIA Electronic Mail
Reference #:
RW2101470
Product:
Tobacco
Recipient:
Recipient Name
Dutch Knudson
Session Supply Company
United States
dutch@sessionsupply.com
Issuing Office:
Center for Tobacco Products
United States
Dear Dutch Knudson:
The United States Food and Drug Administration’s (FDA) Center for Tobacco Products has completed an evaluation of your corrective actions included in your responses dated January 27, 2021 and February 8, 2021, in response to our Warning Letter dated January 15, 2021. Based on our evaluation, it appears that you have taken steps to address the violations contained in the Warning Letter regarding your website https://www.sessionsupply.com.
This letter does not relieve you or your firm from the responsibility of taking all necessary steps to ensure compliance with the Federal Food, Drug, and Cosmetic 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.
Sincerely,
/S/
David Rice
Branch Chief
Division of Promotion, Advertising, and Labeling
Office of Compliance and Enforcement
Center for Tobacco Products
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Google LLC
Google-cloud_compliance@google.com
Content current as of:
06/22/2021
Regulated Product(s)
Tobacco