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Jedyna Sp.

⚠️ Moderate Risk

FEI: 3002633167 • Zamoyskiego 28/30 • POLAND

FEI

FEI Number

3002633167

📍

Location

Zamoyskiego 28/30

🇵🇱

Country

POLAND
🏢

Address

Grupa E. Wedel S.A. Ul., , Zamoyskiego 28/30, , Poland

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
3/21/2003
Latest Refusal
3/21/2003
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
3/21/2003
34GDT07MIXED OR ASSORTED CHOCOLATE CANDIES (BARS, BOXES, LOOSE FORM), WITH NUTS AND FRUIT
11UNSAFE COL
Chicago District Office (CHI-DO)
3/21/2003
34GDT07MIXED OR ASSORTED CHOCOLATE CANDIES (BARS, BOXES, LOOSE FORM), WITH NUTS AND FRUIT
11UNSAFE COL
Chicago District Office (CHI-DO)
3/21/2003
34GDT07MIXED OR ASSORTED CHOCOLATE CANDIES (BARS, BOXES, LOOSE FORM), WITH NUTS AND FRUIT
11UNSAFE COL
Chicago District Office (CHI-DO)

Frequently Asked Questions

What is Jedyna Sp.'s FDA import refusal history?

Jedyna Sp. (FEI: 3002633167) has 3 FDA import refusal record(s) in our database, spanning from 3/21/2003 to 3/21/2003.

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. Jedyna Sp.'s FEI number is 3002633167.

What types of violations has Jedyna Sp. received?

Jedyna Sp. 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 Jedyna Sp. come from?

All FDA import refusal data for Jedyna Sp. 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.