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LABORATORIOS MSD

⚠️ High Risk

FEI: 3032605438 • Ciudad De Mexico • MEXICO

FEI

FEI Number

3032605438

📍

Location

Ciudad De Mexico

🇲🇽

Country

MEXICO
🏢

Address

Av San Jeronimo No 369, , Ciudad De Mexico, , Mexico

High Risk

FDA Import Risk Assessment

51.5
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
11/1/2024
Latest Refusal
11/1/2024
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
11.2×30%
Recency
75.8×20%
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

721×

NEW VET DR

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act in that it appears to be a new animal drug that is unsafe within the meaning of Section 512(a) of the Federal Food, Drug, and Cosmetic Act as it is not the subject of an approved new animal drug application, conditionally approved new animal drug application, or index listing, and no investigational new animal drug exemption applies.

Refusal History

DateProductViolationsDivision
11/1/2024
65RPL99REPLENISHER N.E.C.
72NEW VET DR
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is LABORATORIOS MSD's FDA import refusal history?

LABORATORIOS MSD (FEI: 3032605438) has 1 FDA import refusal record(s) in our database, spanning from 11/1/2024 to 11/1/2024.

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. LABORATORIOS MSD's FEI number is 3032605438.

What types of violations has LABORATORIOS MSD received?

LABORATORIOS MSD 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 LABORATORIOS MSD come from?

All FDA import refusal data for LABORATORIOS MSD 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.