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Alfred Ritter GmbH&Co. KG

✅ Low Risk

FEI: 2000021732 • Waldenbuch, Baden-Wurttemberg • GERMANY

FEI

FEI Number

2000021732

📍

Location

Waldenbuch, Baden-Wurttemberg

🇩🇪

Country

GERMANY
🏢

Address

Alfred-Ritter-Str. 25, , Waldenbuch, Baden-Wurttemberg, Germany

Low Risk

FDA Import Risk Assessment

24.9
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

6
Total Refusals
7
Unique Violations
4/3/2017
Latest Refusal
8/29/2011
Earliest Refusal

Score Breakdown

Violation Severity
36.0×40%
Refusal Volume
31.3×30%
Recency
0.0×20%
Frequency
10.7×10%
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

3242×

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)).

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.

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.

4731×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

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.

2561×

INCONSPICU

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)).

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)].

Refusal History

DateProductViolationsDivision
4/3/2017
34DGT99CHOCOLATE AND CHOCOLATE COVERED CANDY, WITH COCONUT, N.E.C.
482NUTRIT LBL
New Orleans District Office (NOL-DO)
9/5/2013
34FGT01CHOCOLATE CANDY BAR, WITHOUT NUTS AND FRUIT
256INCONSPICU
321LACKS N/C
328USUAL NAME
3320TRANSFAT
482NUTRIT LBL
New Orleans District Office (NOL-DO)
5/16/2013
34KYT04CHOCOLATE BARS
324NO ENGLISH
New Orleans District Office (NOL-DO)
4/10/2013
34CGT01CHOCOLATE CANDY BAR, WITH NUTS OR NUT PRODUCTS (NOT COCONUT)
321LACKS N/C
New Orleans District Office (NOL-DO)
10/7/2011
34FGT01CHOCOLATE CANDY BAR, WITHOUT NUTS AND FRUIT
473LABELING
New Orleans District Office (NOL-DO)
8/29/2011
34FFY99CHOCOLATE AND CHOCOLATE COVERED CANDY, WITHOUT NUTS AND FRUIT, N.E.C.
324NO ENGLISH
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Alfred Ritter GmbH&Co. KG's FDA import refusal history?

Alfred Ritter GmbH&Co. KG (FEI: 2000021732) has 6 FDA import refusal record(s) in our database, spanning from 8/29/2011 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. Alfred Ritter GmbH&Co. KG's FEI number is 2000021732.

What types of violations has Alfred Ritter GmbH&Co. KG received?

Alfred Ritter GmbH&Co. KG 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 Alfred Ritter GmbH&Co. KG come from?

All FDA import refusal data for Alfred Ritter 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.