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Katjes Fassin GmbH + Co KG

⚠️ Moderate Risk

FEI: 3009830722 • Emmerich am Rhein, North Rhine-Westphalia • GERMANY

FEI

FEI Number

3009830722

📍

Location

Emmerich am Rhein, North Rhine-Westphalia

🇩🇪

Country

GERMANY
🏢

Address

Dechant-Sprunken-Str. 53-57, , Emmerich am Rhein, North Rhine-Westphalia, Germany

Moderate Risk

FDA Import Risk Assessment

39.9
LowModerateHighCritical

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

Statistics

22
Total Refusals
8
Unique Violations
4/3/2017
Latest Refusal
1/12/2004
Earliest Refusal

Score Breakdown

Violation Severity
57.7×40%
Refusal Volume
50.4×30%
Recency
0.0×20%
Frequency
16.6×10%
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

1112×

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).

4824×

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.

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)).

3284×

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.

2743×

COLOR LBLG

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

3212×

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.

33201×

TRANSFAT

The product is misbranded under Section 403(q) because the nutrition label does not provide all of the information required by 21 CFR 101.9(c); specifically, the label does not bear the amount of trans fat [21 CFR 101.9(c)(2)(ii)].

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.

Refusal History

DateProductViolationsDivision
4/3/2017
33LGT08LICORICE CANDY, SOFT, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
482NUTRIT LBL
New Orleans District Office (NOL-DO)
5/6/2016
33LGT08LICORICE CANDY, SOFT, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
324NO ENGLISH
482NUTRIT LBL
Philadelphia District Office (PHI-DO)
9/30/2013
33JHT05CANDY BAR OR PIECES (NOT CARAMEL OR FONDANT), SOFT, WITH FRUIT (WITHOUT CHOCOLATE)
321LACKS N/C
328USUAL NAME
3320TRANSFAT
482NUTRIT LBL
New Orleans District Office (NOL-DO)
9/5/2013
33LGT08LICORICE CANDY, SOFT, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
321LACKS N/C
482NUTRIT LBL
New Orleans District Office (NOL-DO)
10/7/2011
33UGT03NOVELTY BUBBLE GUM
324NO ENGLISH
New Orleans District Office (NOL-DO)
10/7/2011
33EGT99HARD CANDY WITHOUT NUTS AND FRUIT, N.E.C. (WITHOUT CHOCOLATE)
324NO ENGLISH
New Orleans District Office (NOL-DO)
8/29/2011
33SYT99CANDY SPECIALTIES, N.E.C. (WITHOUT CHOCOLATE)
324NO ENGLISH
New Orleans District Office (NOL-DO)
7/21/2011
33LGT08LICORICE CANDY, SOFT, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
11UNSAFE COL
274COLOR LBLG
San Francisco District Office (SAN-DO)
7/21/2011
33LDT08LICORICE CANDY, SOFT, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
11UNSAFE COL
274COLOR LBLG
San Francisco District Office (SAN-DO)
7/20/2011
33LGT07JELLIED CANDY, SOFT (JELLY BEANS, GUM DROPS, ETC.), WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
11UNSAFE COL
274COLOR LBLG
San Francisco District Office (SAN-DO)
6/24/2011
33LDT08LICORICE CANDY, SOFT, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
11UNSAFE COL
San Francisco District Office (SAN-DO)
6/24/2011
33LDT08LICORICE CANDY, SOFT, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
11UNSAFE COL
San Francisco District Office (SAN-DO)
6/24/2011
33LDT08LICORICE CANDY, SOFT, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
11UNSAFE COL
San Francisco District Office (SAN-DO)
6/24/2011
33LDT08LICORICE CANDY, SOFT, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
11UNSAFE COL
San Francisco District Office (SAN-DO)
6/24/2011
33LGT07JELLIED CANDY, SOFT (JELLY BEANS, GUM DROPS, ETC.), WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
11UNSAFE COL
San Francisco District Office (SAN-DO)
6/16/2011
33LDT08LICORICE CANDY, SOFT, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
11UNSAFE COL
San Francisco District Office (SAN-DO)
5/26/2011
33LGT07JELLIED CANDY, SOFT (JELLY BEANS, GUM DROPS, ETC.), WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
11UNSAFE COL
San Francisco District Office (SAN-DO)
8/6/2008
33LDT07JELLIED CANDY, SOFT (JELLY BEANS, GUM DROPS, ETC.), WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
11UNSAFE COL
Baltimore District Office (BLT-DO)
8/6/2008
33LDT07JELLIED CANDY, SOFT (JELLY BEANS, GUM DROPS, ETC.), WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
11UNSAFE COL
Baltimore District Office (BLT-DO)
1/12/2004
33LGT08LICORICE CANDY, SOFT, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
328USUAL NAME
Baltimore District Office (BLT-DO)
1/12/2004
33EGT08LICORICE CANDY, HARD, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
328USUAL NAME
Baltimore District Office (BLT-DO)
1/12/2004
33EGT08LICORICE CANDY, HARD, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
218LIST INGRE
328USUAL NAME
Baltimore District Office (BLT-DO)

Frequently Asked Questions

What is Katjes Fassin GmbH + Co KG's FDA import refusal history?

Katjes Fassin GmbH + Co KG (FEI: 3009830722) has 22 FDA import refusal record(s) in our database, spanning from 1/12/2004 to 4/3/2017.

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. Katjes Fassin GmbH + Co KG's FEI number is 3009830722.

What types of violations has Katjes Fassin GmbH + Co KG received?

Katjes Fassin GmbH + Co KG has been cited for 8 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 Katjes Fassin GmbH + Co KG come from?

All FDA import refusal data for Katjes Fassin GmbH + Co KG 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.