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MSD International GmbH

⚠️ Moderate Risk

FEI: 3002808087 • Co. Cork, Cork • IRELAND

FEI

FEI Number

3002808087

📍

Location

Co. Cork, Cork

🇮🇪

Country

IRELAND
🏢

Address

Brinny, Innishannon, Co. Cork, Cork, Ireland

Moderate Risk

FDA Import Risk Assessment

46.0
LowModerateHighCritical

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

Statistics

9
Total Refusals
3
Unique Violations
3/24/2016
Latest Refusal
1/2/2002
Earliest Refusal

Score Breakdown

Violation Severity
85.6×40%
Refusal Volume
37.0×30%
Recency
0.0×20%
Frequency
6.3×10%
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

757×

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).

1181×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

711×

NO LICENSE

The article is subject to refusal of admission under section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) because it appears to be a biological product for which a biologics license is not in effect under the Public Health Service Act, Part F, Subpart 1-Biological Products, Section 351(a), and it is not the subject of an Investigational New Drug application that is in effect. Therefore, it appears to be a new drug under 201(p) of the FD&C Act that it is in violation of section 505(a) of the FD&C Act because it lacks a new drug approval and because it is misbranded under section 502(f)(1)of the FD&C Act because it fails to bear adequate directions for use

Refusal History

DateProductViolationsDivision
3/24/2016
66YCY99EXHIBITS - OTHER DRUG RELATED ITEMS N.E.C.
75UNAPPROVED
Philadelphia District Office (PHI-DO)
3/24/2016
66YCY99EXHIBITS - OTHER DRUG RELATED ITEMS N.E.C.
75UNAPPROVED
Philadelphia District Office (PHI-DO)
3/24/2016
66YCY99EXHIBITS - OTHER DRUG RELATED ITEMS N.E.C.
75UNAPPROVED
Philadelphia District Office (PHI-DO)
11/24/2014
66YCY99EXHIBITS - OTHER DRUG RELATED ITEMS N.E.C.
75UNAPPROVED
Philadelphia District Office (PHI-DO)
11/24/2014
66YCY99EXHIBITS - OTHER DRUG RELATED ITEMS N.E.C.
75UNAPPROVED
Philadelphia District Office (PHI-DO)
5/2/2012
62VCS99ANTI-VIRAL N.E.C.
75UNAPPROVED
New York District Office (NYK-DO)
5/2/2012
62VCS99ANTI-VIRAL N.E.C.
75UNAPPROVED
New York District Office (NYK-DO)
6/25/2003
57CY02INFLUENZA VIRUS VACCINE
71NO LICENSE
Chicago District Office (CHI-DO)
1/2/2002
57CY02INFLUENZA VIRUS VACCINE
118NOT LISTED
Chicago District Office (CHI-DO)

Frequently Asked Questions

What is MSD International GmbH's FDA import refusal history?

MSD International GmbH (FEI: 3002808087) has 9 FDA import refusal record(s) in our database, spanning from 1/2/2002 to 3/24/2016.

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. MSD International GmbH's FEI number is 3002808087.

What types of violations has MSD International GmbH received?

MSD International GmbH has been cited for 3 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 MSD International GmbH come from?

All FDA import refusal data for MSD International GmbH 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.