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Doktorenhof Weinessiggut Wiedemann Gmbh

⚠️ Moderate Risk

FEI: 3001032236 • Venningen, Rhineland-Palatinate • GERMANY

FEI

FEI Number

3001032236

📍

Location

Venningen, Rhineland-Palatinate

🇩🇪

Country

GERMANY
🏢

Address

Raiffeisenstr. 5, , Venningen, Rhineland-Palatinate, Germany

Moderate Risk

FDA Import Risk Assessment

29.7
LowModerateHighCritical

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

Statistics

6
Total Refusals
4
Unique Violations
7/22/2015
Latest Refusal
7/22/2015
Earliest Refusal

Score Breakdown

Violation Severity
35.8×40%
Refusal Volume
31.3×30%
Recency
0.0×20%
Frequency
60.0×10%
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

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.

4735×

LABELING

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

2531×

STD IDENT

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(g)(1) of the FD&C Act in that the article purports to be or is represented as a food for which a definition and standard of identity have been prescribed by regulations as provided by section 401 of the FD&C Act and the article does not conform to such definition and standard.

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.

Refusal History

DateProductViolationsDivision
7/22/2015
27VCI99VINEGAR, N.E.C.
321LACKS N/C
473LABELING
Florida District Office (FLA-DO)
7/22/2015
27VCI99VINEGAR, N.E.C.
321LACKS N/C
473LABELING
Florida District Office (FLA-DO)
7/22/2015
27VCI99VINEGAR, N.E.C.
321LACKS N/C
473LABELING
Florida District Office (FLA-DO)
7/22/2015
27VCI99VINEGAR, N.E.C.
321LACKS N/C
473LABELING
Florida District Office (FLA-DO)
7/22/2015
27VCI99VINEGAR, N.E.C.
321LACKS N/C
328USUAL NAME
Florida District Office (FLA-DO)
7/22/2015
27VCI99VINEGAR, N.E.C.
253STD IDENT
473LABELING
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Doktorenhof Weinessiggut Wiedemann Gmbh's FDA import refusal history?

Doktorenhof Weinessiggut Wiedemann Gmbh (FEI: 3001032236) has 6 FDA import refusal record(s) in our database, spanning from 7/22/2015 to 7/22/2015.

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. Doktorenhof Weinessiggut Wiedemann Gmbh's FEI number is 3001032236.

What types of violations has Doktorenhof Weinessiggut Wiedemann Gmbh received?

Doktorenhof Weinessiggut Wiedemann Gmbh has been cited for 4 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 Doktorenhof Weinessiggut Wiedemann Gmbh come from?

All FDA import refusal data for Doktorenhof Weinessiggut Wiedemann Gmbh 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.