Wyeth Pharmaceuticals Bv
⚠️ Moderate Risk
FEI: 3005059368 • Hoofddorp, Noord-Holland • NETHERLANDS
FEI Number
3005059368
Location
Hoofddorp, Noord-Holland
Country
NETHERLANDSAddress
Planetenweg 99, , Hoofddorp, Noord-Holland, Netherlands
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
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
Frequently Asked Questions
What is Wyeth Pharmaceuticals Bv's FDA import refusal history?
Wyeth Pharmaceuticals Bv (FEI: 3005059368) has 2 FDA import refusal record(s) in our database, spanning from 5/25/2006 to 5/25/2006.
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 Pharmaceuticals Bv's FEI number is 3005059368.
What types of violations has Wyeth Pharmaceuticals Bv received?
Wyeth Pharmaceuticals Bv 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 Pharmaceuticals Bv come from?
All FDA import refusal data for Wyeth Pharmaceuticals Bv 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.