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Teekaram Lakhan

⚠️ Moderate Risk

FEI: 3003314067 • Demarara • GUYANA

FEI

FEI Number

3003314067

📍

Location

Demarara

🇬🇾

Country

GUYANA
🏢

Address

90 Independence Street, , Demarara, , Guyana

Moderate Risk

FDA Import Risk Assessment

45.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
8/29/2002
Latest Refusal
6/7/2002
Earliest Refusal

Score Breakdown

Violation Severity
95.0×40%
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

3081×

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.

91×

SALMONELLA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.

Refusal History

DateProductViolationsDivision
8/29/2002
16AFP99FISH, N.E.C.
9SALMONELLA
New York District Office (NYK-DO)
6/7/2002
16AFP99FISH, N.E.C.
308MFR INSAN
New York District Office (NYK-DO)

Frequently Asked Questions

What is Teekaram Lakhan's FDA import refusal history?

Teekaram Lakhan (FEI: 3003314067) has 2 FDA import refusal record(s) in our database, spanning from 6/7/2002 to 8/29/2002.

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. Teekaram Lakhan's FEI number is 3003314067.

What types of violations has Teekaram Lakhan received?

Teekaram Lakhan has been cited for 2 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 Teekaram Lakhan come from?

All FDA import refusal data for Teekaram Lakhan 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.