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Invitrogen Life Technologies

⚠️ Moderate Risk

FEI: 3004144723 • Auckland • NEW ZEALAND

FEI

FEI Number

3004144723

📍

Location

Auckland

🇳🇿
🏢

Address

502 Penrose, , Auckland, , New Zealand

Moderate Risk

FDA Import Risk Assessment

45.7
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

3
Total Refusals
1
Unique Violations
3/3/2004
Latest Refusal
3/3/2004
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

3083×

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

DateProductViolationsDivision
3/3/2004
88KISSERA, ANIMAL AND HUMAN
308MFR INSAN
New York District Office (NYK-DO)
3/3/2004
88KISSERA, ANIMAL AND HUMAN
308MFR INSAN
New York District Office (NYK-DO)
3/3/2004
88KITMEDIA AND COMPONENTS, SYNTHETIC CELL AND TISSUE CULTURE
308MFR INSAN
New York District Office (NYK-DO)

Frequently Asked Questions

What is Invitrogen Life Technologies's FDA import refusal history?

Invitrogen Life Technologies (FEI: 3004144723) has 3 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 Life Technologies's FEI number is 3004144723.

What types of violations has Invitrogen Life Technologies received?

Invitrogen Life Technologies 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 Life Technologies come from?

All FDA import refusal data for Invitrogen Life Technologies 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.