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Veembedrijf A. Buisman B.V.

⚠️ Moderate Risk

FEI: 3013321125 • Zwolle, Rhineland-Palatinate • NETHERLANDS

FEI

FEI Number

3013321125

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Location

Zwolle, Rhineland-Palatinate

🇳🇱
🏢

Address

Mindenstraat 20, , Zwolle, Rhineland-Palatinate, Netherlands

Moderate Risk

FDA Import Risk Assessment

46.2
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
3/15/2022
Latest Refusal
3/15/2022
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
11.2×30%
Recency
9.4×20%
Frequency
10.0×10%
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

2411×

PESTICIDE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:

Refusal History

DateProductViolationsDivision
3/15/2022
02FFH08GLUTEN, WHEAT
241PESTICIDE
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is Veembedrijf A. Buisman B.V.'s FDA import refusal history?

Veembedrijf A. Buisman B.V. (FEI: 3013321125) has 1 FDA import refusal record(s) in our database, spanning from 3/15/2022 to 3/15/2022.

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. Veembedrijf A. Buisman B.V.'s FEI number is 3013321125.

What types of violations has Veembedrijf A. Buisman B.V. received?

Veembedrijf A. Buisman B.V. has been cited for 1 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 Veembedrijf A. Buisman B.V. come from?

All FDA import refusal data for Veembedrijf A. Buisman B.V. 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.