Atmor Sales and Marketing
⚠️ Moderate Risk
FEI: 3005395775 • Auckland, Auckland • NEW ZEALAND
FEI Number
3005395775
Location
Auckland, Auckland
Country
NEW ZEALANDAddress
Unit 7, 41 Smales Rd; East Tamaki, Auckland, Auckland, New Zealand
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 Atmor Sales and Marketing's FDA import refusal history?
Atmor Sales and Marketing (FEI: 3005395775) has 2 FDA import refusal record(s) in our database, spanning from 8/24/2011 to 8/24/2011.
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. Atmor Sales and Marketing's FEI number is 3005395775.
What types of violations has Atmor Sales and Marketing received?
Atmor Sales and Marketing 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 Atmor Sales and Marketing come from?
All FDA import refusal data for Atmor Sales and Marketing 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.