ALLERGAN
⚠️ Moderate Risk
FEI: 3016867144 • Koeln • GERMANY
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
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).
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/23/2025 | 60QBK07LIDOCAINE | 118NOT LISTED | Division of Northeast Imports (DNEI) |
| 9/23/2025 | 60QBK07LIDOCAINE | 118NOT LISTED | Division of Northeast Imports (DNEI) |
| 9/23/2025 | 60QBK07LIDOCAINE | 118NOT LISTED | Division of Northeast Imports (DNEI) |
| 9/1/2020 | 65QCY02BOTOX | 71NO LICENSE | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is ALLERGAN's FDA import refusal history?
ALLERGAN (FEI: 3016867144) has 4 FDA import refusal record(s) in our database, spanning from 9/1/2020 to 9/23/2025.
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. ALLERGAN's FEI number is 3016867144.
What types of violations has ALLERGAN received?
ALLERGAN 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 ALLERGAN come from?
All FDA import refusal data for ALLERGAN 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.