ImportRefusal LogoImportRefusal

Wyeth Research (UK) Ltd.

⚠️ Moderate Risk

FEI: 3003572844 • Aberdeen • UNITED KINGDOM

FEI

FEI Number

3003572844

📍

Location

Aberdeen

🇬🇧
🏢

Address

Polwarth Building, Foresterhill, Aberdeen, , United Kingdom

Moderate Risk

FDA Import Risk Assessment

43.9
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
11/19/2008
Latest Refusal
5/24/2006
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
12.0×10%
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

753×

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
11/19/2008
61NIY99ANTI-DEPRESSANT N.E.C.
75UNAPPROVED
New York District Office (NYK-DO)
11/19/2008
61NIY99ANTI-DEPRESSANT N.E.C.
75UNAPPROVED
New York District Office (NYK-DO)
5/24/2006
62IIP99ANTI-NEOPLASTIC N.E.C.
75UNAPPROVED
New York District Office (NYK-DO)

Frequently Asked Questions

What is Wyeth Research (UK) Ltd.'s FDA import refusal history?

Wyeth Research (UK) Ltd. (FEI: 3003572844) has 3 FDA import refusal record(s) in our database, spanning from 5/24/2006 to 11/19/2008.

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. Wyeth Research (UK) Ltd.'s FEI number is 3003572844.

What types of violations has Wyeth Research (UK) Ltd. received?

Wyeth Research (UK) Ltd. 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 Wyeth Research (UK) Ltd. come from?

All FDA import refusal data for Wyeth Research (UK) Ltd. 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.