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Lapisa

⚠️ Moderate Risk

FEI: 3003097329 • La Piedad, Michoacan • MEXICO

FEI

FEI Number

3003097329

📍

Location

La Piedad, Michoacan

🇲🇽

Country

MEXICO
🏢

Address

Carr La Piedad Guadalajara Km 5.5, , La Piedad, Michoacan, Mexico

Moderate Risk

FDA Import Risk Assessment

33.1
LowModerateHighCritical

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

Statistics

1
Total Refusals
4
Unique Violations
9/23/2024
Latest Refusal
9/23/2024
Earliest Refusal

Score Breakdown

Violation Severity
35.0×40%
Refusal Volume
11.2×30%
Recency
74.0×20%
Frequency
10.0×10%
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

1181×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

39071×

3907

4721×

NO ENGLISH

Required label or labeling appears to not be in English in violation of 21 C.F.R. 201.15(c)(1).

Refusal History

DateProductViolationsDivision
9/23/2024
65CRP99NUTRIENT/TONIC N.E.C.
118NOT LISTED
3280FRNMFGREG
39073907
472NO ENGLISH
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Lapisa's FDA import refusal history?

Lapisa (FEI: 3003097329) has 1 FDA import refusal record(s) in our database, spanning from 9/23/2024 to 9/23/2024.

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. Lapisa's FEI number is 3003097329.

What types of violations has Lapisa received?

Lapisa has been cited for 4 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 Lapisa come from?

All FDA import refusal data for Lapisa 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.