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IMMO A/S

⚠️ Moderate Risk

FEI: 3020855761 • Vejle, Syddanmark • DENMARK

FEI

FEI Number

3020855761

📍

Location

Vejle, Syddanmark

🇩🇰

Country

DENMARK
🏢

Address

Friis Hansens Vej 9, , Vejle, Syddanmark, Denmark

Moderate Risk

FDA Import Risk Assessment

31.2
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
2/24/2022
Latest Refusal
2/24/2022
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
22.3×30%
Recency
7.3×20%
Frequency
30.0×10%
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

32803×

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
2/24/2022
89ITIWHEELCHAIR, POWERED
3280FRNMFGREG
Division of Northeast Imports (DNEI)
2/24/2022
89ITIWHEELCHAIR, POWERED
3280FRNMFGREG
Division of Northeast Imports (DNEI)
2/24/2022
89ITIWHEELCHAIR, POWERED
3280FRNMFGREG
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is IMMO A/S's FDA import refusal history?

IMMO A/S (FEI: 3020855761) has 3 FDA import refusal record(s) in our database, spanning from 2/24/2022 to 2/24/2022.

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. IMMO A/S's FEI number is 3020855761.

What types of violations has IMMO A/S received?

IMMO A/S 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 IMMO A/S come from?

All FDA import refusal data for IMMO A/S 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.