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C/O NATULIQUE APS

Low Risk

FEI: 3018085354 • Horsens • DENMARK

FEI

FEI Number

3018085354

📍

Location

Horsens

🇩🇰

Country

DENMARK
🏢

Address

Cvr, , Horsens, , Denmark

Low Risk

FDA Import Risk Assessment

23.0
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

1
Total Refusals
3
Unique Violations
4/8/2021
Latest Refusal
4/8/2021
Earliest Refusal

Score Breakdown

Violation Severity
46.7×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

4731×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

4821×

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.

4881×

HEALTH C

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 bears an unauthorized nutrient content/health claim.

Refusal History

DateProductViolationsDivision
4/8/2021
54FYA99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
473LABELING
482NUTRIT LBL
488HEALTH C
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is C/O NATULIQUE APS's FDA import refusal history?

C/O NATULIQUE APS (FEI: 3018085354) has 1 FDA import refusal record(s) in our database, spanning from 4/8/2021 to 4/8/2021.

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. C/O NATULIQUE APS's FEI number is 3018085354.

What types of violations has C/O NATULIQUE APS received?

C/O NATULIQUE APS 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 C/O NATULIQUE APS come from?

All FDA import refusal data for C/O NATULIQUE 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.