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M/S Designwise India Pvt Ltd

⚠️ Moderate Risk

FEI: 3005881704 • Haryana • INDIA

FEI

FEI Number

3005881704

📍

Location

Haryana

🇮🇳

Country

INDIA
🏢

Address

Plot No 400 Pace City Ii, , Haryana, , India

Moderate Risk

FDA Import Risk Assessment

43.3
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
5/2/2012
Latest Refusal
5/31/2007
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
6.1×10%
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

2383×

UNSAFE ADD

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.

Refusal History

DateProductViolationsDivision
5/2/2012
52AID29PLATTERS (FOODWARE, COOKWARE & TABLEWARE)
238UNSAFE ADD
Chicago District Office (CHI-DO)
5/31/2007
52AID28PLATES, ANY SIZE (FOODWARE, COOKWARE & TABLEWARE)
238UNSAFE ADD
Baltimore District Office (BLT-DO)
5/31/2007
52AID28PLATES, ANY SIZE (FOODWARE, COOKWARE & TABLEWARE)
238UNSAFE ADD
Baltimore District Office (BLT-DO)

Frequently Asked Questions

What is M/S Designwise India Pvt Ltd's FDA import refusal history?

M/S Designwise India Pvt Ltd (FEI: 3005881704) has 3 FDA import refusal record(s) in our database, spanning from 5/31/2007 to 5/2/2012.

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. M/S Designwise India Pvt Ltd's FEI number is 3005881704.

What types of violations has M/S Designwise India Pvt Ltd received?

M/S Designwise India Pvt Ltd 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 M/S Designwise India Pvt Ltd come from?

All FDA import refusal data for M/S Designwise India Pvt Ltd 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.