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Lakesida de Mexico, S.A. de C.V.

⚠️ Moderate Risk

FEI: 3003708675 • Toluca • MEXICO

FEI

FEI Number

3003708675

📍

Location

Toluca

🇲🇽

Country

MEXICO
🏢

Address

Via I. Fabela Nte. No. 1536, , Toluca, , Mexico

Moderate Risk

FDA Import Risk Assessment

43.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
2
Unique Violations
2/21/2008
Latest Refusal
5/23/2007
Earliest Refusal

Score Breakdown

Violation Severity
85.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

273×

DRUG GMPS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the methods used in and controls used for the manufacture, processing, packing, or holding of drugs and other products do not appear to conform to current good manufacturing practices within the meaning of Section 501(a)(2)(B).

753×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

Refusal History

DateProductViolationsDivision
2/21/2008
56BCK10BENZYLPENICILLOYL-POLYLYSINE (PENICILLIN, SYNTHETICALLY PRODUCED)
27DRUG GMPS
75UNAPPROVED
Cincinnati District Office (CIN-DO)
7/3/2007
56BCK10BENZYLPENICILLOYL-POLYLYSINE (PENICILLIN, SYNTHETICALLY PRODUCED)
27DRUG GMPS
75UNAPPROVED
Cincinnati District Office (CIN-DO)
5/23/2007
56BDK10BENZYLPENICILLOYL-POLYLYSINE (PENICILLIN, SYNTHETICALLY PRODUCED)
27DRUG GMPS
75UNAPPROVED
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Lakesida de Mexico, S.A. de C.V.'s FDA import refusal history?

Lakesida de Mexico, S.A. de C.V. (FEI: 3003708675) has 3 FDA import refusal record(s) in our database, spanning from 5/23/2007 to 2/21/2008.

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. Lakesida de Mexico, S.A. de C.V.'s FEI number is 3003708675.

What types of violations has Lakesida de Mexico, S.A. de C.V. received?

Lakesida de Mexico, S.A. de C.V. has been cited for 2 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 Lakesida de Mexico, S.A. de C.V. come from?

All FDA import refusal data for Lakesida de Mexico, 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.