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AHLGRENS BILAR /COLETTA AB

⚠️ Moderate Risk

FEI: 3024512087 • Sundbyberg, Stockholms Lan • SWEDEN

FEI

FEI Number

3024512087

📍

Location

Sundbyberg, Stockholms Lan

🇸🇪

Country

SWEDEN
🏢

Address

Landsvagen 50 A, , Sundbyberg, Stockholms Lan, Sweden

Moderate Risk

FDA Import Risk Assessment

35.3
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

1
Total Refusals
1
Unique Violations
10/10/2025
Latest Refusal
10/10/2025
Earliest Refusal

Score Breakdown

Violation Severity
30.0×40%
Refusal Volume
11.2×30%
Recency
94.8×20%
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

3201×

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.

Refusal History

DateProductViolationsDivision
10/10/2025
33SYT99CANDY SPECIALTIES, N.E.C. (WITHOUT CHOCOLATE)
320LACKS FIRM
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is AHLGRENS BILAR /COLETTA AB's FDA import refusal history?

AHLGRENS BILAR /COLETTA AB (FEI: 3024512087) has 1 FDA import refusal record(s) in our database, spanning from 10/10/2025 to 10/10/2025.

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. AHLGRENS BILAR /COLETTA AB's FEI number is 3024512087.

What types of violations has AHLGRENS BILAR /COLETTA AB received?

AHLGRENS BILAR /COLETTA AB has been cited for 1 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 AHLGRENS BILAR /COLETTA AB come from?

All FDA import refusal data for AHLGRENS BILAR /COLETTA AB 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.