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Lonkom International S.A. de C.V.

⚠️ Moderate Risk

FEI: 2000030457 • Juarez, Chihuahua • MEXICO

FEI

FEI Number

2000030457

📍

Location

Juarez, Chihuahua

🇲🇽

Country

MEXICO
🏢

Address

Calle Venezuela Sur 443, Col. Partido Romero, Juarez, Juarez, Chihuahua, Mexico

Moderate Risk

FDA Import Risk Assessment

40.6
LowModerateHighCritical

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

Statistics

6
Total Refusals
3
Unique Violations
12/15/2011
Latest Refusal
4/20/2009
Earliest Refusal

Score Breakdown

Violation Severity
72.5×40%
Refusal Volume
31.3×30%
Recency
0.0×20%
Frequency
22.6×10%
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

835×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

2182×

LIST INGRE

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

2491×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

Refusal History

DateProductViolationsDivision
12/15/2011
24HGT08PEPPER, HOT, DRIED OR PASTE
249FILTHY
Southwest Import District Office (SWI-DO)
11/30/2011
27YCI06PEPPER SAUCE (HOT, MILD, ETC.)
218LIST INGRE
83NO PROCESS
Southwest Import District Office (SWI-DO)
11/30/2011
27YCI06PEPPER SAUCE (HOT, MILD, ETC.)
218LIST INGRE
83NO PROCESS
Southwest Import District Office (SWI-DO)
11/30/2011
27YCI06PEPPER SAUCE (HOT, MILD, ETC.)
83NO PROCESS
Southwest Import District Office (SWI-DO)
11/30/2011
27YCI06PEPPER SAUCE (HOT, MILD, ETC.)
83NO PROCESS
Southwest Import District Office (SWI-DO)
4/20/2009
27YGI06PEPPER SAUCE (HOT, MILD, ETC.)
83NO PROCESS
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

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

Lonkom International S.A. de C.V. (FEI: 2000030457) has 6 FDA import refusal record(s) in our database, spanning from 4/20/2009 to 12/15/2011.

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. Lonkom International S.A. de C.V.'s FEI number is 2000030457.

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

Lonkom International S.A. de C.V. has been cited for 3 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 Lonkom International S.A. de C.V. come from?

All FDA import refusal data for Lonkom International 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.