Adtoit Clinical Supplies
⚠️ Moderate Risk
FEI: 3005717653 • Mount Laurel, NJ • UNITED STATES
FEI Number
3005717653
Location
Mount Laurel, NJ
Country
UNITED STATESAddress
8000 Commerce Pkwy, , Mount Laurel, NJ, 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
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 Adtoit Clinical Supplies's FDA import refusal history?
Adtoit Clinical Supplies (FEI: 3005717653) has 2 FDA import refusal record(s) in our database, spanning from 7/26/2006 to 7/26/2006.
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. Adtoit Clinical Supplies's FEI number is 3005717653.
What types of violations has Adtoit Clinical Supplies received?
Adtoit Clinical Supplies 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 Adtoit Clinical Supplies come from?
All FDA import refusal data for Adtoit Clinical Supplies 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.