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Kaveri Enterprises

⚠️ Moderate Risk

FEI: 3006639856 • Delhi • INDIA

FEI

FEI Number

3006639856

📍

Location

Delhi

🇮🇳

Country

INDIA
🏢

Address

Plot No 334/6, Krishna Market, Pitam Pura Village, Delhi, , India

Moderate Risk

FDA Import Risk Assessment

43.0
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
1/12/2017
Latest Refusal
2/12/2008
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
3.4×10%
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

1973×

COSM COLOR

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a color additive which is unsafe within the meaning of Section 721(a) which renders it adulterated under Section 601(e).

Refusal History

DateProductViolationsDivision
1/12/2017
53YG99OTHER COSMETIC AND COSMETIC PRODUCTS, N.E.C.
197COSM COLOR
Los Angeles District Office (LOS-DO)
2/12/2008
53YH99OTHER COSMETIC AND COSMETIC PRODUCTS, N.E.C.
197COSM COLOR
Seattle District Office (SEA-DO)
2/12/2008
53YG99OTHER COSMETIC AND COSMETIC PRODUCTS, N.E.C.
197COSM COLOR
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is Kaveri Enterprises's FDA import refusal history?

Kaveri Enterprises (FEI: 3006639856) has 3 FDA import refusal record(s) in our database, spanning from 2/12/2008 to 1/12/2017.

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. Kaveri Enterprises's FEI number is 3006639856.

What types of violations has Kaveri Enterprises received?

Kaveri Enterprises 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 Kaveri Enterprises come from?

All FDA import refusal data for Kaveri Enterprises 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.