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Romkell S.P.R. De R.L.

⚠️ Moderate Risk

FEI: 3000955952 • Nuevo Casas Grandes, Chihuahua • MEXICO

FEI

FEI Number

3000955952

📍

Location

Nuevo Casas Grandes, Chihuahua

🇲🇽

Country

MEXICO
🏢

Address

Calle Benito Juarez 2335, Col. OBRERA, Nuevo Casas Grandes, Chihuahua, Mexico

Moderate Risk

FDA Import Risk Assessment

47.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
11/18/2009
Latest Refusal
8/10/2009
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
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

92×

SALMONELLA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.

Refusal History

DateProductViolationsDivision
11/18/2009
24FHB08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE)
9SALMONELLA
Southwest Import District Office (SWI-DO)
8/10/2009
24FHB08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE)
9SALMONELLA
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Romkell S.P.R. De R.L.'s FDA import refusal history?

Romkell S.P.R. De R.L. (FEI: 3000955952) has 2 FDA import refusal record(s) in our database, spanning from 8/10/2009 to 11/18/2009.

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. Romkell S.P.R. De R.L.'s FEI number is 3000955952.

What types of violations has Romkell S.P.R. De R.L. received?

Romkell S.P.R. De R.L. 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 Romkell S.P.R. De R.L. come from?

All FDA import refusal data for Romkell S.P.R. De R.L. 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.