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Wyeth

⚠️ Moderate Risk

FEI: 3005507931 • Montrealmontreal, QUEBEC • CANADA

FEI

FEI Number

3005507931

📍

Location

Montrealmontreal, QUEBEC

🇨🇦

Country

CANADA
🏢

Address

1 Wyeth Canada, , Montrealmontreal, QUEBEC, Canada

Moderate Risk

FDA Import Risk Assessment

40.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
3/13/2013
Latest Refusal
3/29/2011
Earliest Refusal

Score Breakdown

Violation Severity
85.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
10.2×10%
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

721×

NEW VET DR

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act in that it appears to be a new animal drug that is unsafe within the meaning of Section 512(a) of the Federal Food, Drug, and Cosmetic Act as it is not the subject of an approved new animal drug application, conditionally approved new animal drug application, or index listing, and no investigational new animal drug exemption applies.

751×

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
3/13/2013
64LRY24FLUMETHASONE (GLUCOCORTICOID)
72NEW VET DR
Cincinnati District Office (CIN-DO)
3/29/2011
65QDA22METHOCARBAMOL (RELAXANT)
75UNAPPROVED
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Wyeth's FDA import refusal history?

Wyeth (FEI: 3005507931) has 2 FDA import refusal record(s) in our database, spanning from 3/29/2011 to 3/13/2013.

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's FEI number is 3005507931.

What types of violations has Wyeth received?

Wyeth has been cited for 2 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 come from?

All FDA import refusal data for Wyeth 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.