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Euromed SA

⚠️ Moderate Risk

FEI: 3010111275 • Mollet Del Valles, Barcelona • SPAIN

FEI

FEI Number

3010111275

📍

Location

Mollet Del Valles, Barcelona

🇪🇸

Country

SPAIN
🏢

Address

Pol. Ind. Can Magarola, Calle Del Rec De Dalt 21-23, Mollet Del Valles, Barcelona, Spain

Moderate Risk

FDA Import Risk Assessment

43.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
5/7/2012
Latest Refusal
5/1/2012
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

37212×

PESTICIDE2

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be adulterated because it contains a pesticide chemical, which is in violation of section 402(a)(2)(B). Contains:

Refusal History

DateProductViolationsDivision
5/7/2012
54FBT64ST. JOHN'S WORT (HERBAL & BOTANICALS, NOT TEAS)
3721PESTICIDE2
Southwest Import District Office (SWI-DO)
5/1/2012
54FBT64ST. JOHN'S WORT (HERBAL & BOTANICALS, NOT TEAS)
3721PESTICIDE2
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Euromed SA's FDA import refusal history?

Euromed SA (FEI: 3010111275) has 2 FDA import refusal record(s) in our database, spanning from 5/1/2012 to 5/7/2012.

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. Euromed SA's FEI number is 3010111275.

What types of violations has Euromed SA received?

Euromed SA 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 Euromed SA come from?

All FDA import refusal data for Euromed SA 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.