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Intervet Mexico S.A. de C.V. - MSD Animal Health

⚠️ Moderate Risk

FEI: 3002809485 • Ecatepec De Morelos, Mexico • MEXICO

FEI

FEI Number

3002809485

📍

Location

Ecatepec De Morelos, Mexico

🇲🇽

Country

MEXICO
🏢

Address

Plasticos No 28, Santa Clara, Coatitla; Ecatepec De Morelos, Ecatepec De Morelos, Mexico, Mexico

Moderate Risk

FDA Import Risk Assessment

38.3
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

3
Total Refusals
4
Unique Violations
12/19/2023
Latest Refusal
7/19/2011
Earliest Refusal

Score Breakdown

Violation Severity
56.7×40%
Refusal Volume
22.3×30%
Recency
43.6×20%
Frequency
2.4×10%
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

1182×

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).

722×

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.

32601×

NO ENGLISH

Required label or labeling appears to not be in English in violation of 21 C.F.R. 801.15(c)(1)

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

Refusal History

DateProductViolationsDivision
12/19/2023
61KOA44PROPANTHELINE BROMIDE (ANTI-CHOLINERGIC)
118NOT LISTED
3280FRNMFGREG
72NEW VET DR
Division of Southeast Imports (DSEI)
1/24/2017
69BC88ZILPATEROL HYDROCHLORIDE, CATEGORY II, MEDICATED ANIMAL FEED
3260NO ENGLISH
72NEW VET DR
Cincinnati District Office (CIN-DO)
7/19/2011
60WOS14FENBENDAZOLE (ANTHELMINTIC)
118NOT LISTED
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Intervet Mexico S.A. de C.V. - MSD Animal Health's FDA import refusal history?

Intervet Mexico S.A. de C.V. - MSD Animal Health (FEI: 3002809485) has 3 FDA import refusal record(s) in our database, spanning from 7/19/2011 to 12/19/2023.

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. Intervet Mexico S.A. de C.V. - MSD Animal Health's FEI number is 3002809485.

What types of violations has Intervet Mexico S.A. de C.V. - MSD Animal Health received?

Intervet Mexico S.A. de C.V. - MSD Animal Health has been cited for 4 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 Intervet Mexico S.A. de C.V. - MSD Animal Health come from?

All FDA import refusal data for Intervet Mexico S.A. de C.V. - MSD Animal Health 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.