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MUNSTERHUIS

⚠️ High Risk

FEI: 3024341678 • Netherland • NETHERLANDS

FEI

FEI Number

3024341678

📍

Location

Netherland

🇳🇱
🏢

Address

De Bleek 26, , Netherland, , Netherlands

High Risk

FDA Import Risk Assessment

54.3
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

5
Total Refusals
1
Unique Violations
12/5/2022
Latest Refusal
12/5/2022
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
28.8×30%
Recency
23.4×20%
Frequency
50.0×10%
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

1975×

COSM COLOR

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a color additive which is unsafe within the meaning of Section 721(a) which renders it adulterated under Section 601(e).

Refusal History

DateProductViolationsDivision
12/5/2022
50NYY18HENNA
197COSM COLOR
Division of Southeast Imports (DSEI)
12/5/2022
50NYY18HENNA
197COSM COLOR
Division of Southeast Imports (DSEI)
12/5/2022
50NYY18HENNA
197COSM COLOR
Division of Southeast Imports (DSEI)
12/5/2022
50NYY18HENNA
197COSM COLOR
Division of Southeast Imports (DSEI)
12/5/2022
50NYY18HENNA
197COSM COLOR
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is MUNSTERHUIS's FDA import refusal history?

MUNSTERHUIS (FEI: 3024341678) has 5 FDA import refusal record(s) in our database, spanning from 12/5/2022 to 12/5/2022.

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. MUNSTERHUIS's FEI number is 3024341678.

What types of violations has MUNSTERHUIS received?

MUNSTERHUIS 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 MUNSTERHUIS come from?

All FDA import refusal data for MUNSTERHUIS 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.