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Arnime S.A. de C.V.

⚠️ Moderate Risk

FEI: 3004351407 • San Juan Del Rio Del Centauro Del Norte, Durango • MEXICO

FEI

FEI Number

3004351407

📍

Location

San Juan Del Rio Del Centauro Del Norte, Durango

🇲🇽

Country

MEXICO
🏢

Address

Carr. Queretaro Leon Km 63. 8, Col. San Juan Del Rio Del Centauro Del Norte Centro, San Juan Del Rio, San Juan Del Rio Del Centauro Del Norte, Durango, Mexico

Moderate Risk

FDA Import Risk Assessment

40.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
9/13/2011
Latest Refusal
9/13/2011
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
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

29201×

PESTICIDES

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
9/13/2011
24TFD11CELERY (LEAF & STEM VEGETABLE)
2920PESTICIDES
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Arnime S.A. de C.V.'s FDA import refusal history?

Arnime S.A. de C.V. (FEI: 3004351407) has 1 FDA import refusal record(s) in our database, spanning from 9/13/2011 to 9/13/2011.

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. Arnime S.A. de C.V.'s FEI number is 3004351407.

What types of violations has Arnime S.A. de C.V. received?

Arnime S.A. de C.V. 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 Arnime S.A. de C.V. come from?

All FDA import refusal data for Arnime S.A. de C.V. 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.