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NIDIA EDITH S.P.R. DE R.L.

⚠️ Moderate Risk

FEI: 3004902001 • Torreon, Coahuila de Zaragoza • MEXICO

FEI

FEI Number

3004902001

📍

Location

Torreon, Coahuila de Zaragoza

🇲🇽

Country

MEXICO
🏢

Address

Boulevard Diagonal Reforma Ote. Int. A 1798, Col. Torreon Centro, Torreon, Torreon, Coahuila de Zaragoza, Mexico

Moderate Risk

FDA Import Risk Assessment

44.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
10/29/2004
Latest Refusal
10/29/2004
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
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

2411×

PESTICIDE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:

Refusal History

DateProductViolationsDivision
10/29/2004
24FGC08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE)
241PESTICIDE
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is NIDIA EDITH S.P.R. DE R.L.'s FDA import refusal history?

NIDIA EDITH S.P.R. DE R.L. (FEI: 3004902001) has 1 FDA import refusal record(s) in our database, spanning from 10/29/2004 to 10/29/2004.

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. NIDIA EDITH S.P.R. DE R.L.'s FEI number is 3004902001.

What types of violations has NIDIA EDITH S.P.R. DE R.L. received?

NIDIA EDITH 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 NIDIA EDITH S.P.R. DE R.L. come from?

All FDA import refusal data for NIDIA EDITH 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.