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Transmarket Ab

⚠️ Moderate Risk

FEI: 1000539578 • Bankeryd, Jonkopings Lan • SWEDEN

FEI

FEI Number

1000539578

📍

Location

Bankeryd, Jonkopings Lan

🇸🇪

Country

SWEDEN
🏢

Address

Box 136, , Bankeryd, Jonkopings Lan, Sweden

Moderate Risk

FDA Import Risk Assessment

45.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
7/25/2002
Latest Refusal
7/25/2002
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

113×

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).

Refusal History

DateProductViolationsDivision
7/25/2002
33JGY07JELLIED CANDY, SOFT (JELLY BEANS, GUM DROPS, ETC.), WITH FRUIT (WITHOUT CHOCOLATE)
11UNSAFE COL
Minneapolis District Office (MIN-DO)
7/25/2002
33JGY07JELLIED CANDY, SOFT (JELLY BEANS, GUM DROPS, ETC.), WITH FRUIT (WITHOUT CHOCOLATE)
11UNSAFE COL
Minneapolis District Office (MIN-DO)
7/25/2002
33JGY07JELLIED CANDY, SOFT (JELLY BEANS, GUM DROPS, ETC.), WITH FRUIT (WITHOUT CHOCOLATE)
11UNSAFE COL
Minneapolis District Office (MIN-DO)

Frequently Asked Questions

What is Transmarket Ab's FDA import refusal history?

Transmarket Ab (FEI: 1000539578) has 3 FDA import refusal record(s) in our database, spanning from 7/25/2002 to 7/25/2002.

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. Transmarket Ab's FEI number is 1000539578.

What types of violations has Transmarket Ab received?

Transmarket 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 Transmarket Ab come from?

All FDA import refusal data for Transmarket 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.