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Laboratorios Alpharma

⚠️ Moderate Risk

FEI: 3004104228 • Col. Manuel Avila Camacho, Sinaloa • MEXICO

FEI

FEI Number

3004104228

📍

Location

Col. Manuel Avila Camacho, Sinaloa

🇲🇽

Country

MEXICO
🏢

Address

Blvd. Pipila # 1, Navolato, Col. Manuel Avila Camacho, Sinaloa, Mexico

Moderate Risk

FDA Import Risk Assessment

28.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
3
Unique Violations
1/31/2020
Latest Refusal
1/31/2020
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
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

2231×

FALSE

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose labeling appears to be false or misleading.

4721×

NO ENGLISH

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

751×

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
1/31/2020
66VCA99MISCELLANEOUS PATENT MEDICINES, ETC.
223FALSE
472NO ENGLISH
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Laboratorios Alpharma's FDA import refusal history?

Laboratorios Alpharma (FEI: 3004104228) has 1 FDA import refusal record(s) in our database, spanning from 1/31/2020 to 1/31/2020.

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 Alpharma's FEI number is 3004104228.

What types of violations has Laboratorios Alpharma received?

Laboratorios Alpharma 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 Laboratorios Alpharma come from?

All FDA import refusal data for Laboratorios Alpharma 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.