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GHO AHK SPRL

⚠️ High Risk

FEI: 3038629420 • Berrwiller, Haut-Rhin • FRANCE

FEI

FEI Number

3038629420

📍

Location

Berrwiller, Haut-Rhin

🇫🇷

Country

FRANCE
🏢

Address

14 Rue Des Vosges, , Berrwiller, Haut-Rhin, France

High Risk

FDA Import Risk Assessment

52.6
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
10/24/2025
Latest Refusal
10/24/2025
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
11.2×30%
Recency
81.5×20%
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
10/24/2025
66XOY99HOMEOPATHIC N.E.C.
72NEW VET DR
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is GHO AHK SPRL's FDA import refusal history?

GHO AHK SPRL (FEI: 3038629420) has 1 FDA import refusal record(s) in our database, spanning from 10/24/2025 to 10/24/2025.

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. GHO AHK SPRL's FEI number is 3038629420.

What types of violations has GHO AHK SPRL received?

GHO AHK SPRL 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 GHO AHK SPRL come from?

All FDA import refusal data for GHO AHK SPRL 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.