ImportRefusal LogoImportRefusal

Anfele, S.A.

⚠️ High Risk

FEI: 3004676902 • Fuenlabrada, Madrid • SPAIN

FEI

FEI Number

3004676902

📍

Location

Fuenlabrada, Madrid

🇪🇸

Country

SPAIN
🏢

Address

Calle La Baneza 48, , Fuenlabrada, Madrid, Spain

High Risk

FDA Import Risk Assessment

57.4
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
7/21/2025
Latest Refusal
7/21/2025
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
17.7×30%
Recency
90.5×20%
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

25802×

MFRHACCP

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the Act in that it appears to have been prepared, packed or held under insanitary conditions whereby it may have been rendered injurious to health in that it appears to have been processed in violation of 21 CFR 123.6(a) and 123.8(a).

Refusal History

DateProductViolationsDivision
7/21/2025
16AGD01ANCHOVY
2580MFRHACCP
Division of Southeast Imports (DSEI)
7/21/2025
16AGD01ANCHOVY
2580MFRHACCP
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Anfele, S.A.'s FDA import refusal history?

Anfele, S.A. (FEI: 3004676902) has 2 FDA import refusal record(s) in our database, spanning from 7/21/2025 to 7/21/2025.

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. Anfele, S.A.'s FEI number is 3004676902.

What types of violations has Anfele, S.A. received?

Anfele, S.A. 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 Anfele, S.A. come from?

All FDA import refusal data for Anfele, S.A. 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.