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Hemani General Trading LLC

⚠️ Moderate Risk

FEI: 3011161532 • Dubai, Dubai • UNITED ARAB EMIRATES

FEI

FEI Number

3011161532

📍

Location

Dubai, Dubai

🇦🇪
🏢

Address

Al Ras Deira Dubai, , Dubai, Dubai, United Arab Emirates

Moderate Risk

FDA Import Risk Assessment

40.6
LowModerateHighCritical

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

Statistics

7
Total Refusals
5
Unique Violations
8/12/2013
Latest Refusal
11/4/2010
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
33.5×30%
Recency
0.0×20%
Frequency
25.3×10%
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

1974×

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).

3352×

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.

752×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

30001×

N-RX INACT

The article appears to be a nonprescription drug and fails to bear the established name of each inactive ingredient in alphabetical order on the outside container of the retail package.

4711×

CSTIC LBLG

The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.

Refusal History

DateProductViolationsDivision
8/12/2013
53FD01HAIR DYES AND COLORS (ALL TYPES REQUIRE CAUTION STATEMENTS AND PATCH TESTS) (HAIR COLORING PREPARATI
197COSM COLOR
Southwest Import District Office (SWI-DO)
8/12/2013
53FD01HAIR DYES AND COLORS (ALL TYPES REQUIRE CAUTION STATEMENTS AND PATCH TESTS) (HAIR COLORING PREPARATI
197COSM COLOR
Southwest Import District Office (SWI-DO)
8/12/2013
53FD01HAIR DYES AND COLORS (ALL TYPES REQUIRE CAUTION STATEMENTS AND PATCH TESTS) (HAIR COLORING PREPARATI
197COSM COLOR
Southwest Import District Office (SWI-DO)
8/12/2013
50NGY18HENNA
197COSM COLOR
Southwest Import District Office (SWI-DO)
11/4/2010
66VBL99MISCELLANEOUS PATENT MEDICINES, ETC.
3000N-RX INACT
335LACKS N/C
75UNAPPROVED
Minneapolis District Office (MIN-DO)
11/4/2010
53LD03FACE,BODY,AND HAND (EXCLUDING SHAVING PREPARATIONS) (SKIN CARE PREPARATIONS)
471CSTIC LBLG
Minneapolis District Office (MIN-DO)
11/4/2010
66VBL99MISCELLANEOUS PATENT MEDICINES, ETC.
335LACKS N/C
75UNAPPROVED
Minneapolis District Office (MIN-DO)

Frequently Asked Questions

What is Hemani General Trading LLC's FDA import refusal history?

Hemani General Trading LLC (FEI: 3011161532) has 7 FDA import refusal record(s) in our database, spanning from 11/4/2010 to 8/12/2013.

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. Hemani General Trading LLC's FEI number is 3011161532.

What types of violations has Hemani General Trading LLC received?

Hemani General Trading LLC has been cited for 5 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 Hemani General Trading LLC come from?

All FDA import refusal data for Hemani General Trading LLC 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.