Scantibodies Laboratory, Inc.
⚠️ Moderate Risk
FEI: 2020808 • Santee, CA • UNITED STATES
FEI Number
2020808
Location
Santee, CA
Country
UNITED STATESAddress
9336 Abraham Way, , Santee, CA, United States
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
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 |
|---|---|---|---|
| 12/14/2005 | 57DK49HUMAN SERUM ALBUMIN (BLOOD AND BLOOD DERIVATIVES) | 71NO LICENSE | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Scantibodies Laboratory, Inc.'s FDA import refusal history?
Scantibodies Laboratory, Inc. (FEI: 2020808) has 1 FDA import refusal record(s) in our database, spanning from 12/14/2005 to 12/14/2005.
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. Scantibodies Laboratory, Inc.'s FEI number is 2020808.
What types of violations has Scantibodies Laboratory, Inc. received?
Scantibodies Laboratory, Inc. 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 Scantibodies Laboratory, Inc. come from?
All FDA import refusal data for Scantibodies Laboratory, Inc. 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.