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DGF INDUSTRIES

⚠️ Moderate Risk

FEI: 3013484136 • Chanteloup Les Vignes, Yvelines • FRANCE

FEI

FEI Number

3013484136

📍

Location

Chanteloup Les Vignes, Yvelines

🇫🇷

Country

FRANCE
🏢

Address

Zone Industrielle Des Cettons 2, 7 Rue Henri Navier, Chanteloup Les Vignes, Yvelines, France

Moderate Risk

FDA Import Risk Assessment

36.9
LowModerateHighCritical

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

Statistics

6
Total Refusals
6
Unique Violations
1/9/2018
Latest Refusal
8/28/2003
Earliest Refusal

Score Breakdown

Violation Severity
67.8×40%
Refusal Volume
31.3×30%
Recency
0.0×20%
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

623×

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).

112×

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).

2181×

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.

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.

4821×

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.

831×

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.

Refusal History

DateProductViolationsDivision
1/9/2018
21SEE07PINEAPPLE (SUBTROPICAL AND TROPICAL FRUIT)
218LIST INGRE
321LACKS N/C
482NUTRIT LBL
83NO PROCESS
Division of Northeast Imports (DNEI)
3/29/2006
16MEE14SNAILS, AQUATIC, OTHER AQUATIC SPECIES
62NEEDS FCE
Chicago District Office (CHI-DO)
3/29/2006
23DGE11PISTACHIO, PASTE
62NEEDS FCE
Chicago District Office (CHI-DO)
3/29/2006
23DEE04CHESTNUT, PASTE
62NEEDS FCE
Chicago District Office (CHI-DO)
8/28/2003
21LGT01APRICOT, TOPPING OR SYRUP
11UNSAFE COL
Los Angeles District Office (LOS-DO)
8/28/2003
21LGT01APRICOT, TOPPING OR SYRUP
11UNSAFE COL
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is DGF INDUSTRIES's FDA import refusal history?

DGF INDUSTRIES (FEI: 3013484136) has 6 FDA import refusal record(s) in our database, spanning from 8/28/2003 to 1/9/2018.

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. DGF INDUSTRIES's FEI number is 3013484136.

What types of violations has DGF INDUSTRIES received?

DGF INDUSTRIES has been cited for 6 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 DGF INDUSTRIES come from?

All FDA import refusal data for DGF INDUSTRIES 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.