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Dochorse

⚠️ Moderate Risk

FEI: 3009261644 • Utrecht, Utrecht • NETHERLANDS

FEI

FEI Number

3009261644

📍

Location

Utrecht, Utrecht

🇳🇱
🏢

Address

Otto Hahnweg 24, , Utrecht, Utrecht, Netherlands

Moderate Risk

FDA Import Risk Assessment

36.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
11/21/2016
Latest Refusal
11/21/2016
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
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

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
11/21/2016
68YBJ02HORSES ANIMAL DRUGS N.E.C.
72NEW VET DR
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Dochorse's FDA import refusal history?

Dochorse (FEI: 3009261644) has 1 FDA import refusal record(s) in our database, spanning from 11/21/2016 to 11/21/2016.

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. Dochorse's FEI number is 3009261644.

What types of violations has Dochorse received?

Dochorse 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 Dochorse come from?

All FDA import refusal data for Dochorse 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.