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Clara Luhanga

⚠️ Moderate Risk

FEI: 3003740137 • Dar • TANZANIA

FEI

FEI Number

3003740137

📍

Location

Dar

🇹🇿

Country

TANZANIA
🏢

Address

P.O. Box 13962, , Dar, , Tanzania

Moderate Risk

FDA Import Risk Assessment

33.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
10/10/2002
Latest Refusal
10/10/2002
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
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

1793×

AGR RX

The article appears to be a prescription drug manufactured in the U.S. and offered for import by other than the manufacturer and reimportation does not appear to have been authorized by the Secretary for use in a medical emergency.

Refusal History

DateProductViolationsDivision
10/10/2002
62GCC99ANTI-INFLAMMATORY N.E.C.
179AGR RX
New Orleans District Office (NOL-DO)
10/10/2002
56BCB03AMOXICILLIN TRIHYDRATE (PENICILLIN, SYNTHETICALLY PRODUCED)
179AGR RX
New Orleans District Office (NOL-DO)
10/10/2002
56BCC05AMPICILLIN (PENICILLIN, SYNTHETICALLY PRODUCED)
179AGR RX
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Clara Luhanga's FDA import refusal history?

Clara Luhanga (FEI: 3003740137) has 3 FDA import refusal record(s) in our database, spanning from 10/10/2002 to 10/10/2002.

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. Clara Luhanga's FEI number is 3003740137.

What types of violations has Clara Luhanga received?

Clara Luhanga 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 Clara Luhanga come from?

All FDA import refusal data for Clara Luhanga 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.