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BIOMEP S.A DE CV

⚠️ High Risk

FEI: 3013769535 • Juarez • MEXICO

FEI

FEI Number

3013769535

📍

Location

Juarez

🇲🇽

Country

MEXICO
🏢

Address

Parque Industrial Nauca, , Juarez, , Mexico

High Risk

FDA Import Risk Assessment

60.7
LowModerateHighCritical

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

Statistics

4
Total Refusals
1
Unique Violations
3/6/2025
Latest Refusal
11/29/2021
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
25.9×30%
Recency
78.5×20%
Frequency
12.2×10%
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

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
3/6/2025
61KDY99ANTI-CHOLINERGIC, N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/17/2024
64BCB24FUROSEMIDE (DIURETIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
2/27/2024
64BCB24FUROSEMIDE (DIURETIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
11/29/2021
62VCY18ACYCLOVIR (ANTI-VIRAL)
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is BIOMEP S.A DE CV's FDA import refusal history?

BIOMEP S.A DE CV (FEI: 3013769535) has 4 FDA import refusal record(s) in our database, spanning from 11/29/2021 to 3/6/2025.

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. BIOMEP S.A DE CV's FEI number is 3013769535.

What types of violations has BIOMEP S.A DE CV received?

BIOMEP S.A DE CV 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 BIOMEP S.A DE CV come from?

All FDA import refusal data for BIOMEP S.A DE CV 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.