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Pottson Enterprise

⚠️ Moderate Risk

FEI: 1000332906 • Whakatane New Zealand • NEW ZEALAND

FEI

FEI Number

1000332906

📍

Location

Whakatane New Zealand

🇳🇿
🏢

Address

235 Domain Rd., , Whakatane New Zealand, , New Zealand

Moderate Risk

FDA Import Risk Assessment

47.2
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
6/28/2005
Latest Refusal
6/15/2004
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
19.3×10%
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

2412×

PESTICIDE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:

Refusal History

DateProductViolationsDivision
6/28/2005
21SHC12PASSION FRUIT (SUBTROPICAL AND TROPICAL FRUIT)
241PESTICIDE
Los Angeles District Office (LOS-DO)
6/15/2004
21SHC12PASSION FRUIT (SUBTROPICAL AND TROPICAL FRUIT)
241PESTICIDE
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Pottson Enterprise's FDA import refusal history?

Pottson Enterprise (FEI: 1000332906) has 2 FDA import refusal record(s) in our database, spanning from 6/15/2004 to 6/28/2005.

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. Pottson Enterprise's FEI number is 1000332906.

What types of violations has Pottson Enterprise received?

Pottson Enterprise 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 Pottson Enterprise come from?

All FDA import refusal data for Pottson Enterprise 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.