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Ness Technologies

⚠️ Moderate Risk

FEI: 3004989127 • Bangalore • INDIA

FEI

FEI Number

3004989127

📍

Location

Bangalore

🇮🇳

Country

INDIA
🏢

Address

Ii Floor Salapuria Citadel, , Bangalore, , India

Moderate Risk

FDA Import Risk Assessment

25.7
LowModerateHighCritical

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

Statistics

1
Total Refusals
3
Unique Violations
3/29/2005
Latest Refusal
3/29/2005
Earliest Refusal

Score Breakdown

Violation Severity
53.3×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

3351×

LACKS N/C

The article is in package form and appears to not have a label containing an accurate statement of the quantity of the contents in terms of weight, measure or numerical count and no variations or exemptions have been prescribed by regs.

3421×

PERSONALRX

The article appears to be a drug which requires a prescription from your doctor.

4831×

DRUG NAME

The article appears to be a drug and fails to bear the proprietary or established name and/or name and quantity of each active ingredient.

Refusal History

DateProductViolationsDivision
3/29/2005
66VCP99MISCELLANEOUS PATENT MEDICINES, ETC.
335LACKS N/C
342PERSONALRX
483DRUG NAME
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Ness Technologies's FDA import refusal history?

Ness Technologies (FEI: 3004989127) has 1 FDA import refusal record(s) in our database, spanning from 3/29/2005 to 3/29/2005.

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. Ness Technologies's FEI number is 3004989127.

What types of violations has Ness Technologies received?

Ness Technologies has been cited for 3 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 Ness Technologies come from?

All FDA import refusal data for Ness Technologies 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.