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TAMARAPU GEETHA DEVI

⚠️ High Risk

FEI: 3039431372 • Palakonda, Andhra Pradesh • INDIA

FEI

FEI Number

3039431372

📍

Location

Palakonda, Andhra Pradesh

🇮🇳

Country

INDIA
🏢

Address

245 Konchada Veedhi, D No 1, Palakonda, Andhra Pradesh, India

High Risk

FDA Import Risk Assessment

66.0
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

3
Total Refusals
1
Unique Violations
10/27/2025
Latest Refusal
10/27/2025
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
22.3×30%
Recency
81.7×20%
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

2493×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

Refusal History

DateProductViolationsDivision
10/27/2025
21SYH14TAMARIND (SUBTROPICAL AND TROPICAL FRUIT)
249FILTHY
Division of Southeast Imports (DSEI)
10/27/2025
21SYH14TAMARIND (SUBTROPICAL AND TROPICAL FRUIT)
249FILTHY
Division of Southeast Imports (DSEI)
10/27/2025
21SYH14TAMARIND (SUBTROPICAL AND TROPICAL FRUIT)
249FILTHY
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is TAMARAPU GEETHA DEVI's FDA import refusal history?

TAMARAPU GEETHA DEVI (FEI: 3039431372) has 3 FDA import refusal record(s) in our database, spanning from 10/27/2025 to 10/27/2025.

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. TAMARAPU GEETHA DEVI's FEI number is 3039431372.

What types of violations has TAMARAPU GEETHA DEVI received?

TAMARAPU GEETHA DEVI 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 TAMARAPU GEETHA DEVI come from?

All FDA import refusal data for TAMARAPU GEETHA DEVI 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.