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MED PHARMA LABORATORY

⚠️ High Risk

FEI: 3030171112 • Guatemala, Guatemala • GUATEMALA

FEI

FEI Number

3030171112

📍

Location

Guatemala, Guatemala

🇬🇹

Country

GUATEMALA
🏢

Address

Calle Bodegas, 1-10 Z, Guatemala, Guatemala, Guatemala

High Risk

FDA Import Risk Assessment

57.0
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
1/21/2026
Latest Refusal
8/25/2024
Earliest Refusal

Score Breakdown

Violation Severity
76.7×40%
Refusal Volume
17.7×30%
Recency
97.9×20%
Frequency
14.2×10%
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

752×

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).

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).

Refusal History

DateProductViolationsDivision
1/21/2026
66VDK99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
75UNAPPROVED
Division of Southeast Imports (DSEI)
8/25/2024
54AGY99VITAMIN, N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is MED PHARMA LABORATORY's FDA import refusal history?

MED PHARMA LABORATORY (FEI: 3030171112) has 2 FDA import refusal record(s) in our database, spanning from 8/25/2024 to 1/21/2026.

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. MED PHARMA LABORATORY's FEI number is 3030171112.

What types of violations has MED PHARMA LABORATORY received?

MED PHARMA LABORATORY has been cited for 2 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 MED PHARMA LABORATORY come from?

All FDA import refusal data for MED PHARMA LABORATORY 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.