ImportRefusal LogoImportRefusal

Ramon Guillen E Hijos

⚠️ Moderate Risk

FEI: 1000176946 • La Algaida-Archena, Murcia • SPAIN

FEI

FEI Number

1000176946

📍

Location

La Algaida-Archena, Murcia

🇪🇸

Country

SPAIN
🏢

Address

R.M. De Murcia Libro 175 Seccion 2folio, , La Algaida-Archena, Murcia, Spain

Moderate Risk

FDA Import Risk Assessment

36.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
3/19/2002
Latest Refusal
3/19/2002
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
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

831×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

Refusal History

DateProductViolationsDivision
3/19/2002
25YEE99VEGETABLE & VEGETABLE PRODUCTS NOT MENTIONED ELSEWHERE, N.E.C.
83NO PROCESS
Baltimore District Office (BLT-DO)

Frequently Asked Questions

What is Ramon Guillen E Hijos's FDA import refusal history?

Ramon Guillen E Hijos (FEI: 1000176946) has 1 FDA import refusal record(s) in our database, spanning from 3/19/2002 to 3/19/2002.

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. Ramon Guillen E Hijos's FEI number is 1000176946.

What types of violations has Ramon Guillen E Hijos received?

Ramon Guillen E Hijos 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 Ramon Guillen E Hijos come from?

All FDA import refusal data for Ramon Guillen E Hijos 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.