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LABORATORIOS FINLAY

⚠️ Moderate Risk

FEI: 3021727728 • Tegucigalpa, Francisco Morazan • HONDURAS

FEI

FEI Number

3021727728

📍

Location

Tegucigalpa, Francisco Morazan

🇭🇳

Country

HONDURAS
🏢

Address

Blvd.Kuwait ,Col Las Vegas, , Tegucigalpa, Francisco Morazan, Honduras

Moderate Risk

FDA Import Risk Assessment

25.8
LowModerateHighCritical

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

Statistics

1
Total Refusals
5
Unique Violations
4/21/2022
Latest Refusal
4/21/2022
Earliest Refusal

Score Breakdown

Violation Severity
48.0×40%
Refusal Volume
11.2×30%
Recency
11.4×20%
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

2181×

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.

3201×

LACKS FIRM

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(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.

3211×

LACKS N/C

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(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.

3281×

USUAL NAME

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)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.

Refusal History

DateProductViolationsDivision
4/21/2022
54AYL05VITAMIN B12 (CYANOCOBALAMIN)
218LIST INGRE
249FILTHY
320LACKS FIRM
321LACKS N/C
328USUAL NAME
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is LABORATORIOS FINLAY's FDA import refusal history?

LABORATORIOS FINLAY (FEI: 3021727728) has 1 FDA import refusal record(s) in our database, spanning from 4/21/2022 to 4/21/2022.

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. LABORATORIOS FINLAY's FEI number is 3021727728.

What types of violations has LABORATORIOS FINLAY received?

LABORATORIOS FINLAY has been cited for 5 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 LABORATORIOS FINLAY come from?

All FDA import refusal data for LABORATORIOS FINLAY 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.