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H.K. EXPORTS

⚠️ High Risk

FEI: 3010326532 • Ahmedabad, Gujarat • INDIA

FEI

FEI Number

3010326532

📍

Location

Ahmedabad, Gujarat

🇮🇳

Country

INDIA
🏢

Address

98 Keshavnagar Co Op Society, , Ahmedabad, Gujarat, India

High Risk

FDA Import Risk Assessment

53.9
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

5
Total Refusals
8
Unique Violations
9/10/2024
Latest Refusal
12/14/2021
Earliest Refusal

Score Breakdown

Violation Severity
71.8×40%
Refusal Volume
28.8×30%
Recency
73.3×20%
Frequency
18.2×10%
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

113×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

38782×

POISONORD

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a poisonous or deleterious substance which would ordinarily render the article injurious to health. Contains:

2381×

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.

24611×

UNSFDIETUS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a dietary supplement or contain a dietary ingredient that renders it adulterated under section 402(a)(1) under the conditions of use recommended or suggested in the labeling of such dietary supplement.

2741×

COLOR LBLG

The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.

3201×

LACKS FIRM

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.

3281×

USUAL NAME

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.

2181×

LIST INGRE

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

Refusal History

DateProductViolationsDivision
9/10/2024
23BGT14BETEL NUT, SHELLED
238UNSAFE ADD
2461UNSFDIETUS
320LACKS FIRM
328USUAL NAME
3878POISONORD
Division of Northeast Imports (DNEI)
8/27/2024
23BGT14BETEL NUT, SHELLED
3878POISONORD
Division of Northeast Imports (DNEI)
8/7/2024
28EGT99MIXED SPICE AND SEAONINGS, WITHOUT SALT, N.E.C.
11UNSAFE COL
Division of Northeast Imports (DNEI)
12/9/2022
28EGT99MIXED SPICE AND SEAONINGS, WITHOUT SALT, N.E.C.
11UNSAFE COL
Division of Northeast Imports (DNEI)
12/14/2021
28EGT99MIXED SPICE AND SEAONINGS, WITHOUT SALT, N.E.C.
11UNSAFE COL
218LIST INGRE
274COLOR LBLG
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is H.K. EXPORTS's FDA import refusal history?

H.K. EXPORTS (FEI: 3010326532) has 5 FDA import refusal record(s) in our database, spanning from 12/14/2021 to 9/10/2024.

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. H.K. EXPORTS's FEI number is 3010326532.

What types of violations has H.K. EXPORTS received?

H.K. EXPORTS has been cited for 8 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 H.K. EXPORTS come from?

All FDA import refusal data for H.K. EXPORTS 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.