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Droga Kolinska, Zivilska industrija d. d.

⚠️ Moderate Risk

FEI: 3013259039 • Ljubljana, Ljubljana (Urbane Commune) • SLOVENIA

FEI

FEI Number

3013259039

📍

Location

Ljubljana, Ljubljana (Urbane Commune)

🇸🇮

Country

SLOVENIA
🏢

Address

Kolinska Ulica 1, , Ljubljana, Ljubljana (Urbane Commune), Slovenia

Moderate Risk

FDA Import Risk Assessment

46.6
LowModerateHighCritical

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

Statistics

8
Total Refusals
9
Unique Violations
6/5/2025
Latest Refusal
5/22/2006
Earliest Refusal

Score Breakdown

Violation Severity
45.0×40%
Refusal Volume
35.3×30%
Recency
88.0×20%
Frequency
4.2×10%
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

3244×

NO ENGLISH

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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

2182×

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.

3202×

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.

832×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

4822×

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.

3281×

USUAL NAME

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)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.

20401×

SULFITELBL

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded because 1) it appears to contain sulfites but the label fails to declare the presence of sulfites, a fact material to sulfite-sensitive individuals who must avoid the ingredient due to potential health consequences from its consumption, and 2) it appears the food is fabricated from two or more ingredients and the label does not list the common or usual name of each ingredient.

621×

NEEDS FCE

It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).

3211×

LACKS N/C

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)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.

Refusal History

DateProductViolationsDivision
6/5/2025
54BBY08MAGNESIUM (MINERAL)
324NO ENGLISH
Division of Southeast Imports (DSEI)
6/5/2025
54BBY08MAGNESIUM (MINERAL)
218LIST INGRE
324NO ENGLISH
Division of Southeast Imports (DSEI)
4/25/2025
54BBY08MAGNESIUM (MINERAL)
324NO ENGLISH
Division of Southeast Imports (DSEI)
5/18/2017
40PET01MILK BASE INFANT FORMULA PRODUCT (0-12 MONTHS), POWDER FORMULA
320LACKS FIRM
324NO ENGLISH
Division of West Coast Imports (DWCI)
9/17/2010
16AEE45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
482NUTRIT LBL
83NO PROCESS
Detroit District Office (DET-DO)
1/29/2008
27YYY04HORSERADISH, PREPARED
2040SULFITELBL
Chicago District Office (CHI-DO)
1/29/2008
29WGY02BOTTLED SPRING OR MINERAL WATER
218LIST INGRE
320LACKS FIRM
321LACKS N/C
328USUAL NAME
482NUTRIT LBL
Chicago District Office (CHI-DO)
5/22/2006
16AEE45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
62NEEDS FCE
83NO PROCESS
Chicago District Office (CHI-DO)

Frequently Asked Questions

What is Droga Kolinska, Zivilska industrija d. d.'s FDA import refusal history?

Droga Kolinska, Zivilska industrija d. d. (FEI: 3013259039) has 8 FDA import refusal record(s) in our database, spanning from 5/22/2006 to 6/5/2025.

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. Droga Kolinska, Zivilska industrija d. d.'s FEI number is 3013259039.

What types of violations has Droga Kolinska, Zivilska industrija d. d. received?

Droga Kolinska, Zivilska industrija d. d. has been cited for 9 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 Droga Kolinska, Zivilska industrija d. d. come from?

All FDA import refusal data for Droga Kolinska, Zivilska industrija d. d. 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.