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MENDI INNOVATIONS AB

⚠️ Moderate Risk

FEI: 3038172257 • Stockholm, Stockholms Lan • SWEDEN

FEI

FEI Number

3038172257

📍

Location

Stockholm, Stockholms Lan

🇸🇪

Country

SWEDEN
🏢

Address

Ostermalmsgatan 26a, , Stockholm, Stockholms Lan, Sweden

Moderate Risk

FDA Import Risk Assessment

42.1
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
6/23/2025
Latest Refusal
6/23/2025
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
11.2×30%
Recency
89.0×20%
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

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
6/23/2025
84HCCDEVICE, BIOFEEDBACK
3280FRNMFGREG
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is MENDI INNOVATIONS AB's FDA import refusal history?

MENDI INNOVATIONS AB (FEI: 3038172257) has 1 FDA import refusal record(s) in our database, spanning from 6/23/2025 to 6/23/2025.

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. MENDI INNOVATIONS AB's FEI number is 3038172257.

What types of violations has MENDI INNOVATIONS AB received?

MENDI INNOVATIONS AB 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 MENDI INNOVATIONS AB come from?

All FDA import refusal data for MENDI INNOVATIONS AB 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.