Jens Moller Products ApS
⚠️ Moderate Risk
FEI: 3009211710 • Herning, Midtjylland • DENMARK
FEI Number
3009211710
Location
Herning, Midtjylland
Country
DENMARKAddress
Hi-Park 411, , Herning, Midtjylland, Denmark
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
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
LACKS FIRM
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.
LACKS N/C
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.
NUTRIT LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.
NO PROCESS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.
UNSAFE COL
The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).
USUAL NAME
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/5/2015 | 24THE29SEAWEED (LEAF & STEM VEGETABLE) | Baltimore District Office (BLT-DO) | |
| 1/5/2015 | 24THE29SEAWEED (LEAF & STEM VEGETABLE) | Baltimore District Office (BLT-DO) | |
| 1/5/2015 | 24THE29SEAWEED (LEAF & STEM VEGETABLE) | Baltimore District Office (BLT-DO) | |
| 1/5/2015 | 24THE29SEAWEED (LEAF & STEM VEGETABLE) | Baltimore District Office (BLT-DO) | |
| 1/5/2015 | 24THE29SEAWEED (LEAF & STEM VEGETABLE) | Baltimore District Office (BLT-DO) | |
| 1/5/2015 | 24THE29SEAWEED (LEAF & STEM VEGETABLE) | Baltimore District Office (BLT-DO) |
Frequently Asked Questions
What is Jens Moller Products ApS's FDA import refusal history?
Jens Moller Products ApS (FEI: 3009211710) has 6 FDA import refusal record(s) in our database, spanning from 1/5/2015 to 1/5/2015.
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. Jens Moller Products ApS's FEI number is 3009211710.
What types of violations has Jens Moller Products ApS received?
Jens Moller Products ApS has been cited for 6 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 Jens Moller Products ApS come from?
All FDA import refusal data for Jens Moller Products ApS 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.