Droga Kolinska, Zivilska industrija d. d.
⚠️ Moderate Risk
FEI: 3013259039 • Ljubljana, Ljubljana (Urbane Commune) • SLOVENIA
FEI Number
3013259039
Location
Ljubljana, Ljubljana (Urbane Commune)
Country
SLOVENIAAddress
Kolinska Ulica 1, , Ljubljana, Ljubljana (Urbane Commune), Slovenia
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
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)).
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.
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.
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.
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.
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.
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.
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).
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 6/5/2025 | 54BBY08MAGNESIUM (MINERAL) | 324NO ENGLISH | Division of Southeast Imports (DSEI) |
| 6/5/2025 | 54BBY08MAGNESIUM (MINERAL) | 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 | Division of West Coast Imports (DWCI) | |
| 9/17/2010 | 16AEE45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | Detroit District Office (DET-DO) | |
| 1/29/2008 | 27YYY04HORSERADISH, PREPARED | 2040SULFITELBL | Chicago District Office (CHI-DO) |
| 1/29/2008 | 29WGY02BOTTLED SPRING OR MINERAL WATER | Chicago District Office (CHI-DO) | |
| 5/22/2006 | 16AEE45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | 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.