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Merck Sharp & Dohme (I.A.) Corp

⚠️ Moderate Risk

FEI: 3008159568 • Selangorselangor • MALAYSIA

FEI

FEI Number

3008159568

📍

Location

Selangorselangor

🇲🇾

Country

MALAYSIA
🏢

Address

T2-9 Jaya 33 No. 33 (Lot 33)Jalan, , Selangorselangor, , Malaysia

Moderate Risk

FDA Import Risk Assessment

43.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
12/30/2011
Latest Refusal
12/30/2011
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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
12/30/2011
61ECB09MONTELUKAST SODIUM (ANTI-ASTHMATIC)
75UNAPPROVED
New Orleans District Office (NOL-DO)
12/30/2011
55RP31MICROCRYSTALLINE CELLULOSE (PHARMACEUTIC NECESSITY - TABLET & CAPSULE DILUENT)
75UNAPPROVED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Merck Sharp & Dohme (I.A.) Corp's FDA import refusal history?

Merck Sharp & Dohme (I.A.) Corp (FEI: 3008159568) has 2 FDA import refusal record(s) in our database, spanning from 12/30/2011 to 12/30/2011.

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. Merck Sharp & Dohme (I.A.) Corp's FEI number is 3008159568.

What types of violations has Merck Sharp & Dohme (I.A.) Corp received?

Merck Sharp & Dohme (I.A.) Corp 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 & Dohme (I.A.) Corp come from?

All FDA import refusal data for Merck Sharp & Dohme (I.A.) Corp 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.