NICOPODS EHF
⚠️ High Risk
FEI: 3032766412 • Sudurnesjabar • ICELAND
FEI Number
3032766412
Location
Sudurnesjabar
Country
ICELANDAddress
Idngardar 4a, , Sudurnesjabar, , Iceland
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
UNAPPROVED
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).
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).
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
FRNMFGREG
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.
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.
TPNICWARN
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 appears to be misbranded under section 903(a)(7)(B) in that it is sold or distributed in violation of regulations prescribed under 906(d), namely its package fails to bear the required warning statement "WARNING: This product contains nicotine. Nicotine is an addictive chemical." Or if applicable the required statement "This product is made from tobacco."
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/18/2025 | 98NBA11NICOTINE POUCH | Division of Southeast Imports (DSEI) | |
| 12/18/2025 | 98NBA11NICOTINE POUCH | Division of Southeast Imports (DSEI) | |
| 12/15/2025 | 98NCA99NICOTINE DELIVERY PRODUCT, NEC | Division of Southeast Imports (DSEI) | |
| 12/1/2025 | 98NBA11NICOTINE POUCH | 3842TP NO PMTA | Division of Southeast Imports (DSEI) |
| 12/1/2025 | 98NBA11NICOTINE POUCH | 3842TP NO PMTA | Division of Southeast Imports (DSEI) |
| 12/1/2025 | 98NBA11NICOTINE POUCH | 3842TP NO PMTA | Division of Southeast Imports (DSEI) |
| 11/10/2025 | 98NCA99NICOTINE DELIVERY PRODUCT, NEC | 3842TP NO PMTA | Division of Southeast Imports (DSEI) |
| 10/31/2025 | 98NCA99NICOTINE DELIVERY PRODUCT, NEC | Division of Southeast Imports (DSEI) | |
| 10/31/2025 | 98NCA99NICOTINE DELIVERY PRODUCT, NEC | Division of Southeast Imports (DSEI) | |
| 10/30/2025 | 66BAY44NICOTINE DELIVERY SYSTEM | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 10/24/2025 | 54AAR99VITAMIN, N.E.C. | 75UNAPPROVED | Division of Northeast Imports (DNEI) |
| 10/9/2025 | 98NCA99NICOTINE DELIVERY PRODUCT, NEC | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 9/30/2025 | 98NCA11NICOTINE POUCH | 75UNAPPROVED | Division of Northeast Imports (DNEI) |
| 9/30/2025 | 98NCA99NICOTINE DELIVERY PRODUCT, NEC | 75UNAPPROVED | Division of Northeast Imports (DNEI) |
| 9/18/2025 | 98NCA11NICOTINE POUCH | Division of Northeast Imports (DNEI) | |
| 9/12/2025 | 98NCA11NICOTINE POUCH | 75UNAPPROVED | Division of Northeast Imports (DNEI) |
| 8/27/2025 | 98NCA11NICOTINE POUCH | 75UNAPPROVED | Division of Northeast Imports (DNEI) |
| 8/21/2025 | 98NCA11NICOTINE POUCH | 3842TP NO PMTA | Division of Southeast Imports (DSEI) |
| 8/21/2025 | 98NCA99NICOTINE DELIVERY PRODUCT, NEC | 75UNAPPROVED | Division of Northeast Imports (DNEI) |
| 8/20/2025 | 98NCA11NICOTINE POUCH | 3842TP NO PMTA | Division of Southeast Imports (DSEI) |
| 8/18/2025 | 98NCA11NICOTINE POUCH | Division of Northeast Imports (DNEI) | |
| 8/5/2025 | 98NAA11NICOTINE POUCH | Division of Northeast Imports (DNEI) | |
| 6/18/2025 | 66BAY44NICOTINE DELIVERY SYSTEM | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 2/7/2025 | 54ABR99VITAMIN, N.E.C. | Division of Southeast Imports (DSEI) | |
| 2/7/2025 | 54ABR99VITAMIN, N.E.C. | Division of Southeast Imports (DSEI) | |
| 2/7/2025 | 54ABR99VITAMIN, N.E.C. | Division of Southeast Imports (DSEI) | |
| 2/7/2025 | 54ABR99VITAMIN, N.E.C. | Division of Southeast Imports (DSEI) | |
| 2/7/2025 | 60XAY99ANTI-ADRENERGIC, N.E.C. | Division of Southeast Imports (DSEI) | |
| 2/7/2025 | 60XAY99ANTI-ADRENERGIC, N.E.C. | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is NICOPODS EHF's FDA import refusal history?
NICOPODS EHF (FEI: 3032766412) has 29 FDA import refusal record(s) in our database, spanning from 2/7/2025 to 12/18/2025.
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. NICOPODS EHF's FEI number is 3032766412.
What types of violations has NICOPODS EHF received?
NICOPODS EHF has been cited for 7 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 NICOPODS EHF come from?
All FDA import refusal data for NICOPODS EHF 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.