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Jutrzenka S.A.

⚠️ Moderate Risk

FEI: 3001225482 • Bydgoszcz, Kujawsko-Pomorskie • POLAND

FEI

FEI Number

3001225482

📍

Location

Bydgoszcz, Kujawsko-Pomorskie

🇵🇱

Country

POLAND
🏢

Address

Ul. Tadeusza Kosciuszki 53, , Bydgoszcz, Kujawsko-Pomorskie, Poland

Moderate Risk

FDA Import Risk Assessment

38.9
LowModerateHighCritical

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

Statistics

10
Total Refusals
3
Unique Violations
5/17/2013
Latest Refusal
10/21/2005
Earliest Refusal

Score Breakdown

Violation Severity
65.0×40%
Refusal Volume
38.6×30%
Recency
0.0×20%
Frequency
13.2×10%
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

115×

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).

2184×

LIST INGRE

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)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

2741×

COLOR LBLG

The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.

Refusal History

DateProductViolationsDivision
5/17/2013
21KDT01APRICOT, JUICE, PIT FRUIT JUICES OR CONCENTRATES
11UNSAFE COL
Division of Northeast Imports (DNEI)
5/17/2013
20DHT05CURRANTS, BLACK, JUICE OR CONCENTRATES
11UNSAFE COL
Division of Northeast Imports (DNEI)
1/30/2013
20DDT05CURRANTS, BLACK, JUICE OR CONCENTRATES
274COLOR LBLG
Division of Northeast Imports (DNEI)
1/30/2013
21KDT01APRICOT, JUICE, PIT FRUIT JUICES OR CONCENTRATES
218LIST INGRE
Division of Northeast Imports (DNEI)
1/30/2013
20SDT99CORE FRUIT JUICES OR CONCENTRATES, N.E.C.
218LIST INGRE
Division of Northeast Imports (DNEI)
9/23/2008
34GGT02CHOCOLATE CANDY PIECES, WITH NUTS AND FRUIT
218LIST INGRE
Chicago District Office (CHI-DO)
9/23/2008
34EGT01CHOCOLATE CANDY BAR, WITH FRUIT AND FRUIT PRODUCTS
218LIST INGRE
Chicago District Office (CHI-DO)
4/10/2006
33CFT06FLAVORED CANDY, HARD (LIVE SAVERS, ETC.), WITH FRUIT (WITHOUT CHOCOLATE)
11UNSAFE COL
Chicago District Office (CHI-DO)
12/2/2005
33CFT06FLAVORED CANDY, HARD (LIVE SAVERS, ETC.), WITH FRUIT (WITHOUT CHOCOLATE)
11UNSAFE COL
Chicago District Office (CHI-DO)
10/21/2005
33CFT06FLAVORED CANDY, HARD (LIVE SAVERS, ETC.), WITH FRUIT (WITHOUT CHOCOLATE)
11UNSAFE COL
Chicago District Office (CHI-DO)

Frequently Asked Questions

What is Jutrzenka S.A.'s FDA import refusal history?

Jutrzenka S.A. (FEI: 3001225482) has 10 FDA import refusal record(s) in our database, spanning from 10/21/2005 to 5/17/2013.

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. Jutrzenka S.A.'s FEI number is 3001225482.

What types of violations has Jutrzenka S.A. received?

Jutrzenka S.A. 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 Jutrzenka S.A. come from?

All FDA import refusal data for Jutrzenka S.A. 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.