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LAMFER LAB

⚠️ High Risk

FEI: 3025977006 • San Juan • GUATEMALA

FEI

FEI Number

3025977006

📍

Location

San Juan

🇬🇹

Country

GUATEMALA
🏢

Address

Km 16 5 Carretera A, , San Juan, , Guatemala

High Risk

FDA Import Risk Assessment

53.9
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

4
Total Refusals
1
Unique Violations
4/24/2023
Latest Refusal
4/24/2023
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
25.9×30%
Recency
30.8×20%
Frequency
40.0×10%
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

754×

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
4/24/2023
60LDY01ACETAMINOPHEN (ANALGESIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
4/24/2023
61WDY18MICONAZOLE NITRATE (ANTI-FUNGAL) (NOT ANTIBIOTIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
4/24/2023
61HDY03TRIMETHOPRIM (ANTI-BACTERIAL)
75UNAPPROVED
Division of Southeast Imports (DSEI)
4/24/2023
61HDY03TRIMETHOPRIM (ANTI-BACTERIAL)
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is LAMFER LAB's FDA import refusal history?

LAMFER LAB (FEI: 3025977006) has 4 FDA import refusal record(s) in our database, spanning from 4/24/2023 to 4/24/2023.

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. LAMFER LAB's FEI number is 3025977006.

What types of violations has LAMFER LAB received?

LAMFER LAB has been cited for 1 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 LAMFER LAB come from?

All FDA import refusal data for LAMFER LAB 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.