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Nimagen B.V.

⚠️ Moderate Risk

FEI: 3011302238 • Nijmegen, Gelderland • NETHERLANDS

FEI

FEI Number

3011302238

📍

Location

Nijmegen, Gelderland

🇳🇱
🏢

Address

Lagelandseweg 56, , Nijmegen, Gelderland, Netherlands

Moderate Risk

FDA Import Risk Assessment

28.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
4/3/2019
Latest Refusal
4/3/2019
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
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

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

Refusal History

DateProductViolationsDivision
4/3/2019
88PPMGENERAL PURPOSE REAGENT
16DIRECTIONS
3280FRNMFGREG
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is Nimagen B.V.'s FDA import refusal history?

Nimagen B.V. (FEI: 3011302238) has 1 FDA import refusal record(s) in our database, spanning from 4/3/2019 to 4/3/2019.

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. Nimagen B.V.'s FEI number is 3011302238.

What types of violations has Nimagen B.V. received?

Nimagen B.V. has been cited for 2 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 Nimagen B.V. come from?

All FDA import refusal data for Nimagen 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.