ImportRefusal LogoImportRefusal

Dis

⚠️ Moderate Risk

FEI: 3003996173 • Sittard, Limburg • NETHERLANDS

FEI

FEI Number

3003996173

📍

Location

Sittard, Limburg

🇳🇱
🏢

Address

Dr. Nolenslaan 106, , Sittard, Limburg, Netherlands

Moderate Risk

FDA Import Risk Assessment

40.0
LowModerateHighCritical

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

Statistics

9
Total Refusals
7
Unique Violations
12/20/2024
Latest Refusal
9/4/2019
Earliest Refusal

Score Breakdown

Violation Severity
35.6×40%
Refusal Volume
37.0×30%
Recency
64.6×20%
Frequency
17.0×10%
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

3246×

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)).

3215×

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.

4825×

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.

3203×

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.

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.

111×

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).

38651×

COLORLABEL

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.

Refusal History

DateProductViolationsDivision
12/20/2024
29BYY09SOFT DRINK, OTHER FRUIT FLAVORED, CARBONATED
321LACKS N/C
324NO ENGLISH
Division of Northeast Imports (DNEI)
11/5/2024
29BYY09SOFT DRINK, OTHER FRUIT FLAVORED, CARBONATED
218LIST INGRE
Division of Northeast Imports (DNEI)
10/2/2023
29BCY50SOFT DRINK, COLA, CARBONATED
320LACKS FIRM
321LACKS N/C
324NO ENGLISH
482NUTRIT LBL
Division of Northeast Imports (DNEI)
10/2/2023
29BCY09SOFT DRINK, OTHER FRUIT FLAVORED, CARBONATED
320LACKS FIRM
321LACKS N/C
324NO ENGLISH
482NUTRIT LBL
Division of Northeast Imports (DNEI)
10/2/2023
29BCY09SOFT DRINK, OTHER FRUIT FLAVORED, CARBONATED
320LACKS FIRM
321LACKS N/C
324NO ENGLISH
482NUTRIT LBL
Division of Northeast Imports (DNEI)
10/26/2022
29BYY09SOFT DRINK, OTHER FRUIT FLAVORED, CARBONATED
11UNSAFE COL
Division of Southeast Imports (DSEI)
12/2/2021
29BYY09SOFT DRINK, OTHER FRUIT FLAVORED, CARBONATED
218LIST INGRE
321LACKS N/C
3865COLORLABEL
482NUTRIT LBL
Division of Southeast Imports (DSEI)
9/20/2019
29BET20SOFT DRINK, ROOT FLAVORED (ROOT BEER, GINGER ALE, ETC.), CARBONATED
324NO ENGLISH
Division of Southeast Imports (DSEI)
9/4/2019
29BET20SOFT DRINK, ROOT FLAVORED (ROOT BEER, GINGER ALE, ETC.), CARBONATED
324NO ENGLISH
482NUTRIT LBL
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Dis's FDA import refusal history?

Dis (FEI: 3003996173) has 9 FDA import refusal record(s) in our database, spanning from 9/4/2019 to 12/20/2024.

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. Dis's FEI number is 3003996173.

What types of violations has Dis received?

Dis has been cited for 7 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 Dis come from?

All FDA import refusal data for Dis 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.