Storz & Bickel GmbH & Co. KG
⚠️ High Risk
FEI: 3013216814 • Tuttlingen, Baden-Wurttemberg • GERMANY
FEI Number
3013216814
Location
Tuttlingen, Baden-Wurttemberg
Country
GERMANYAddress
In Grubenacker 5-9, , Tuttlingen, Baden-Wurttemberg, Germany
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
Statistics
Score Breakdown
How is this score calculated?
Proprietary Algorithm
- 40% Violation Severity — AI-assessed (1-10)
- 30% Refusal Volume — Logarithmic scale
- 20% Recency — Decays over 5 years
- 10% Frequency — Refusals per year
© ImportRefusal.com Original Analysis
Violation Summary
TP NO PMTA
This article is subject to refusal of admission pursuant to section 801(a)(3) of the FD&C Act because it is a tobacco product that FDA has found to be adulterated under section 902(6)(A) of the FD&C Act in that it does not have an FDA marketing order in effect under section 910(c)(1)(A)(i) of the FD&C Act.
TP NO SE
This article is subject to refusal of admission pursuant to section 801(a)(3) of the FD&C Act because it is a tobacco product that FDA has found to be misbranded under section 903(a)(6) of the FD&C Act in that a notice or other information respecting it was not provided as required by section 905(j).
TPLKUSSLLB
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act because it is a tobacco product in package form that appears to be misbranded under section 903(a)(2)(D) of the FD&C Act in that the label does not provide the statement "sale only allowed in the United States" and the tobacco product is not subject to any exemptions or variations.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 5/12/2025 | 98LEA09ADVANCED PERSONAL VAPORIZER | Division of Southeast Imports (DSEI) | |
| 5/12/2025 | 98LEA09ADVANCED PERSONAL VAPORIZER | Division of Southeast Imports (DSEI) | |
| 5/12/2025 | 98LEA09ADVANCED PERSONAL VAPORIZER | Division of Southeast Imports (DSEI) | |
| 5/12/2025 | 98LEA09ADVANCED PERSONAL VAPORIZER | Division of Southeast Imports (DSEI) | |
| 5/12/2025 | 98LEA09ADVANCED PERSONAL VAPORIZER | Division of Southeast Imports (DSEI) | |
| 5/12/2025 | 98LEA09ADVANCED PERSONAL VAPORIZER | Division of Southeast Imports (DSEI) | |
| 5/12/2025 | 98LEA09ADVANCED PERSONAL VAPORIZER | Division of Southeast Imports (DSEI) | |
| 5/12/2025 | 98LEA09ADVANCED PERSONAL VAPORIZER | Division of Southeast Imports (DSEI) | |
| 3/27/2024 | 98MEA99ELECTRONIC NICOTINE DELIVERY SYSTEM COMPONENT/PART, NEC | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is Storz & Bickel GmbH & Co. KG's FDA import refusal history?
Storz & Bickel GmbH & Co. KG (FEI: 3013216814) has 9 FDA import refusal record(s) in our database, spanning from 3/27/2024 to 5/12/2025.
What is an FEI number?
FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. Storz & Bickel GmbH & Co. KG's FEI number is 3013216814.
What types of violations has Storz & Bickel GmbH & Co. KG received?
Storz & Bickel GmbH & Co. KG has been cited for 3 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.
Where does this information about Storz & Bickel GmbH & Co. KG come from?
All FDA import refusal data for Storz & Bickel GmbH & Co. KG is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.
Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.