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UNIPHARM

⚠️ High Risk

FEI: 3016791547 • Guatemala, Guatemala • GUATEMALA

FEI

FEI Number

3016791547

📍

Location

Guatemala, Guatemala

🇬🇹

Country

GUATEMALA
🏢

Address

12 Calle 2-25 Z. 10, , Guatemala, Guatemala, Guatemala

High Risk

FDA Import Risk Assessment

63.0
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
12/22/2025
Latest Refusal
5/29/2020
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
22.3×30%
Recency
99.0×20%
Frequency
5.4×10%
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

753×

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
12/22/2025
61XCL08CHLORPHENIRAMINE MALEATE (ANTI-HISTAMINIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/3/2021
56ACL99PENICILLIN NATURAL, N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)
5/29/2020
61PCA26METFORMIN (ANTI-DIABETIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is UNIPHARM's FDA import refusal history?

UNIPHARM (FEI: 3016791547) has 3 FDA import refusal record(s) in our database, spanning from 5/29/2020 to 12/22/2025.

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. UNIPHARM's FEI number is 3016791547.

What types of violations has UNIPHARM received?

UNIPHARM 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 UNIPHARM come from?

All FDA import refusal data for UNIPHARM 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.