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Kohenoor Intl

⚠️ Moderate Risk

FEI: 3007839721 • Hyderabad • PAKISTAN

FEI

FEI Number

3007839721

📍

Location

Hyderabad

🇵🇰

Country

PAKISTAN
🏢

Address

1/2 1336 Old Subzi Market, , Hyderabad, , Pakistan

Moderate Risk

FDA Import Risk Assessment

40.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
10/15/2009
Latest Refusal
10/15/2009
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
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

31201×

EPHEDALK

The product is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a dietary supplement or a dietary ingredient that appears to contain ephedrine alkaloids, which presents an unreasonable risk of illness or injury under the conditions of use recommended or suggested in the labeling, or if no conditions of use are suggested in the labeling, under ordinary conditions of use.

Refusal History

DateProductViolationsDivision
10/15/2009
54YYY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
3120EPHEDALK
New York District Office (NYK-DO)

Frequently Asked Questions

What is Kohenoor Intl's FDA import refusal history?

Kohenoor Intl (FEI: 3007839721) has 1 FDA import refusal record(s) in our database, spanning from 10/15/2009 to 10/15/2009.

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. Kohenoor Intl's FEI number is 3007839721.

What types of violations has Kohenoor Intl received?

Kohenoor Intl 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 Kohenoor Intl come from?

All FDA import refusal data for Kohenoor Intl 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.