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MEDPHARMA

⚠️ High Risk

FEI: 3017178027 • Guatemala • GUATEMALA

FEI

FEI Number

3017178027

📍

Location

Guatemala

🇬🇹

Country

GUATEMALA
🏢

Address

13 Calle 1-10, , Guatemala, , Guatemala

High Risk

FDA Import Risk Assessment

61.0
LowModerateHighCritical

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

Statistics

4
Total Refusals
1
Unique Violations
9/23/2025
Latest Refusal
8/17/2022
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
25.9×30%
Recency
79.7×20%
Frequency
12.9×10%
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
9/23/2025
54AGL13VITAMIN C (ASCORBIC ACID)
75UNAPPROVED
Division of Southeast Imports (DSEI)
9/23/2025
54AFE13VITAMIN C (ASCORBIC ACID)
75UNAPPROVED
Division of Southeast Imports (DSEI)
8/25/2024
56YDY99ANTIBIOTIC N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)
8/17/2022
56BCE03AMOXICILLIN TRIHYDRATE (PENICILLIN, SYNTHETICALLY PRODUCED)
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is MEDPHARMA's FDA import refusal history?

MEDPHARMA (FEI: 3017178027) has 4 FDA import refusal record(s) in our database, spanning from 8/17/2022 to 9/23/2025.

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. MEDPHARMA's FEI number is 3017178027.

What types of violations has MEDPHARMA received?

MEDPHARMA 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 MEDPHARMA come from?

All FDA import refusal data for MEDPHARMA 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.