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AMCA PRODUCE SPR DE RL DE CV

⚠️ Moderate Risk

FEI: 3013606403 • San Luis Rio Colorado, Sonora • MEXICO

FEI

FEI Number

3013606403

📍

Location

San Luis Rio Colorado, Sonora

🇲🇽

Country

MEXICO
🏢

Address

Callejon Miguel Hidalgo Y Costilla 1412, Barrio Residencias, San Luis Rio Colorado, Sonora, 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
3/18/2019
Latest Refusal
3/15/2019
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

2412×

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
3/18/2019
24TFC46CILANTRO (LEAF & STEM VEGETABLE)
241PESTICIDE
Division of Southwest Imports (DSWI)
3/15/2019
24TFC46CILANTRO (LEAF & STEM VEGETABLE)
241PESTICIDE
Division of Southwest Imports (DSWI)

Frequently Asked Questions

What is AMCA PRODUCE SPR DE RL DE CV's FDA import refusal history?

AMCA PRODUCE SPR DE RL DE CV (FEI: 3013606403) has 2 FDA import refusal record(s) in our database, spanning from 3/15/2019 to 3/18/2019.

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. AMCA PRODUCE SPR DE RL DE CV's FEI number is 3013606403.

What types of violations has AMCA PRODUCE SPR DE RL DE CV received?

AMCA PRODUCE SPR DE RL DE CV 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 AMCA PRODUCE SPR DE RL DE CV come from?

All FDA import refusal data for AMCA PRODUCE SPR DE RL DE CV 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.