ImportRefusal LogoImportRefusal

Hul Kin SA de CV

⚠️ Moderate Risk

FEI: 3011279942 • Celestun, Yucatan • MEXICO

FEI

FEI Number

3011279942

📍

Location

Celestun, Yucatan

🇲🇽

Country

MEXICO
🏢

Address

Calle 29 Nro 109a, Celestun, Celestun, Yucatan, Mexico

Moderate Risk

FDA Import Risk Assessment

47.5
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
3/11/2009
Latest Refusal
4/11/2005
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
7.7×10%
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

93×

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
3/11/2009
16MGD09OCTOPUS, OTHER AQUATIC SPECIES
9SALMONELLA
Southwest Import District Office (SWI-DO)
3/11/2009
16MGD09OCTOPUS, OTHER AQUATIC SPECIES
9SALMONELLA
Southwest Import District Office (SWI-DO)
4/11/2005
16MGD09OCTOPUS, OTHER AQUATIC SPECIES
9SALMONELLA
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Hul Kin SA de CV's FDA import refusal history?

Hul Kin SA de CV (FEI: 3011279942) has 3 FDA import refusal record(s) in our database, spanning from 4/11/2005 to 3/11/2009.

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. Hul Kin SA de CV's FEI number is 3011279942.

What types of violations has Hul Kin SA de CV received?

Hul Kin SA 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 Hul Kin SA de CV come from?

All FDA import refusal data for Hul Kin SA 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.