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Merck Sharp And Dohme De

⚠️ Moderate Risk

FEI: 3003041652 • Caracas, D.F. • VENEZUELA

FEI

FEI Number

3003041652

📍

Location

Caracas, D.F.

🇻🇪

Country

VENEZUELA
🏢

Address

Centro Empresarial Senderos 1, , Caracas, D.F., Venezuela

Moderate Risk

FDA Import Risk Assessment

42.4
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
8/27/2007
Latest Refusal
11/2/2005
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
11.0×10%
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

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
8/27/2007
61JDP14SIMVASTATIN (ANTI-CHOLESTEREMIC)
75UNAPPROVED
New Orleans District Office (NOL-DO)
11/2/2005
60XCK23TIMOLOL MALEATE (ANTI-ADRENERGIC)
75UNAPPROVED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Merck Sharp And Dohme De's FDA import refusal history?

Merck Sharp And Dohme De (FEI: 3003041652) has 2 FDA import refusal record(s) in our database, spanning from 11/2/2005 to 8/27/2007.

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. Merck Sharp And Dohme De's FEI number is 3003041652.

What types of violations has Merck Sharp And Dohme De received?

Merck Sharp And Dohme De 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 Merck Sharp And Dohme De come from?

All FDA import refusal data for Merck Sharp And Dohme De 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.