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Vizcaino Hnos

⚠️ Moderate Risk

FEI: 3005056948 • Guadalajara, Jalisco • MEXICO

FEI

FEI Number

3005056948

📍

Location

Guadalajara, Jalisco

🇲🇽

Country

MEXICO
🏢

Address

calle 10 No. 1006, MDO. de Abastos, Guadalajara, Jalisco, Mexico

Moderate Risk

FDA Import Risk Assessment

47.2
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
4/19/2006
Latest Refusal
3/28/2005
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
18.9×10%
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
4/19/2006
24TGC31LETTUCE, HEAD (E.G. ICEBERG) (LEAF & STEM VEGETABLE)
241PESTICIDE
Southwest Import District Office (SWI-DO)
3/28/2005
24TFC31LETTUCE, HEAD (E.G. ICEBERG) (LEAF & STEM VEGETABLE)
241PESTICIDE
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Vizcaino Hnos's FDA import refusal history?

Vizcaino Hnos (FEI: 3005056948) has 2 FDA import refusal record(s) in our database, spanning from 3/28/2005 to 4/19/2006.

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. Vizcaino Hnos's FEI number is 3005056948.

What types of violations has Vizcaino Hnos received?

Vizcaino Hnos 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 Vizcaino Hnos come from?

All FDA import refusal data for Vizcaino Hnos 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.