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Merk Sharp & Dohme

⚠️ Moderate Risk

FEI: 3003374081 • Uccle, Bruxelles-capitale • BELGIUM

FEI

FEI Number

3003374081

📍

Location

Uccle, Bruxelles-capitale

🇧🇪

Country

BELGIUM
🏢

Address

Chaussee De Waterloo 1135, , Uccle, Bruxelles-capitale, Belgium

Moderate Risk

FDA Import Risk Assessment

42.2
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
12/12/2011
Latest Refusal
10/17/2009
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
9.3×10%
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

752×

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
12/12/2011
61GCA84NORFLOXACIN (ANTI-BACTERIAL, PART II) (NOT ANTIBIOTIC)
75UNAPPROVED
New Orleans District Office (NOL-DO)
10/17/2009
62OCK26DORZOLAMIDE HYDROCHLORIDE (ANTI-HYPERTENSIVE - PART II)
75UNAPPROVED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Merk Sharp & Dohme's FDA import refusal history?

Merk Sharp & Dohme (FEI: 3003374081) has 2 FDA import refusal record(s) in our database, spanning from 10/17/2009 to 12/12/2011.

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. Merk Sharp & Dohme's FEI number is 3003374081.

What types of violations has Merk Sharp & Dohme received?

Merk Sharp & Dohme 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 Merk Sharp & Dohme come from?

All FDA import refusal data for Merk Sharp & Dohme 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.