INSURGENT VENTURES III
⚠️ High Risk
FEI: 3025082062 • Gentofte, Hovedstaden • DENMARK
FEI Number
3025082062
Location
Gentofte, Hovedstaden
Country
DENMARKAddress
Sandtoften 9, , Gentofte, Hovedstaden, Denmark
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.
TPNOWRNLBL
This article is subject to refusal of admission pursuant to section 801(a)(3) of the FD&C Act in that it is a tobacco product which appears to be misbranded under section 903(a)(8)(B)(i) and 903(a)(1) because its package label does not include a brief statement of the relevant warnings (i.e., one of the four warnings required by section 3 of the Comprehensive Smokeless Tobacco Health Education Act).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/27/2025 | 98NCA11NICOTINE POUCH | Division of Southeast Imports (DSEI) | |
| 10/22/2025 | 98NBA11NICOTINE POUCH | 3842TP NO PMTA | Division of Southeast Imports (DSEI) |
| 9/24/2025 | 98NCA11NICOTINE POUCH | Division of West Coast Imports (DWCI) | |
| 9/23/2025 | 98NBA11NICOTINE POUCH | Division of Southeast Imports (DSEI) | |
| 8/26/2025 | 98NCA11NICOTINE POUCH | 3854TPLKUSSLLB | Division of Southeast Imports (DSEI) |
| 7/23/2025 | 98NCA11NICOTINE POUCH | Division of Southeast Imports (DSEI) | |
| 5/13/2025 | 98NCA99NICOTINE DELIVERY PRODUCT, NEC | Division of Northeast Imports (DNEI) | |
| 4/22/2025 | 98NCA99NICOTINE DELIVERY PRODUCT, NEC | Division of Southeast Imports (DSEI) | |
| 4/2/2025 | 98NCA99NICOTINE DELIVERY PRODUCT, NEC | Division of Southeast Imports (DSEI) | |
| 3/21/2024 | 98CCA06SNUS | 3854TPLKUSSLLB | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is INSURGENT VENTURES III's FDA import refusal history?
INSURGENT VENTURES III (FEI: 3025082062) has 10 FDA import refusal record(s) in our database, spanning from 3/21/2024 to 10/27/2025.
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. INSURGENT VENTURES III's FEI number is 3025082062.
What types of violations has INSURGENT VENTURES III received?
INSURGENT VENTURES III has been cited for 4 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 INSURGENT VENTURES III come from?
All FDA import refusal data for INSURGENT VENTURES III 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.