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Teresa Lewis

⚠️ Moderate Risk

FEI: 3003465637 • Kingston • JAMAICA

FEI

FEI Number

3003465637

📍

Location

Kingston

🇯🇲

Country

JAMAICA
🏢

Address

188 Spanish Town Road, , Kingston, , Jamaica

Moderate Risk

FDA Import Risk Assessment

39.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
11/3/2004
Latest Refusal
10/21/2004
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

832×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

Refusal History

DateProductViolationsDivision
11/3/2004
24TEY99LEAF & STEM VEGETABLES, N.E.C.
83NO PROCESS
New York District Office (NYK-DO)
10/21/2004
29WYY01BOTTLED WATER
83NO PROCESS
New York District Office (NYK-DO)

Frequently Asked Questions

What is Teresa Lewis's FDA import refusal history?

Teresa Lewis (FEI: 3003465637) has 2 FDA import refusal record(s) in our database, spanning from 10/21/2004 to 11/3/2004.

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. Teresa Lewis's FEI number is 3003465637.

What types of violations has Teresa Lewis received?

Teresa Lewis 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 Teresa Lewis come from?

All FDA import refusal data for Teresa Lewis 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.