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MEDIPRODUCTS GUATEMALA ABSONS SA

⚠️ Moderate Risk

FEI: 3015214118 • San Miguel Peta • GUATEMALA

FEI

FEI Number

3015214118

📍

Location

San Miguel Peta

🇬🇹

Country

GUATEMALA
🏢

Address

Calle Real 17-80 Zona 1, , San Miguel Peta, , Guatemala

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
2
Unique Violations
4/2/2019
Latest Refusal
4/2/2019
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

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
4/2/2019
62GCD42INDOMETHACIN (ANTI-INFLAMMATORY)
472NO ENGLISH
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is MEDIPRODUCTS GUATEMALA ABSONS SA's FDA import refusal history?

MEDIPRODUCTS GUATEMALA ABSONS SA (FEI: 3015214118) has 1 FDA import refusal record(s) in our database, spanning from 4/2/2019 to 4/2/2019.

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. MEDIPRODUCTS GUATEMALA ABSONS SA's FEI number is 3015214118.

What types of violations has MEDIPRODUCTS GUATEMALA ABSONS SA received?

MEDIPRODUCTS GUATEMALA ABSONS SA 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 MEDIPRODUCTS GUATEMALA ABSONS SA come from?

All FDA import refusal data for MEDIPRODUCTS GUATEMALA ABSONS SA 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.