Invitrogen New Zealand Limited
⚠️ Moderate Risk
FEI: 3003339861 • New Zealand • NEW ZEALAND
FEI Number
3003339861
Location
New Zealand
Country
NEW ZEALANDAddress
P.O. Box# 12-502 Penrose, , Auckland, New Zealand, , 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
MFR INSAN
The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.
Refusal History
Frequently Asked Questions
What is Invitrogen New Zealand Limited's FDA import refusal history?
Invitrogen New Zealand Limited (FEI: 3003339861) has 2 FDA import refusal record(s) in our database, spanning from 3/3/2004 to 3/3/2004.
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. Invitrogen New Zealand Limited's FEI number is 3003339861.
What types of violations has Invitrogen New Zealand Limited received?
Invitrogen New Zealand Limited 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 Invitrogen New Zealand Limited come from?
All FDA import refusal data for Invitrogen New Zealand Limited 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.