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ABRA WHOLESALE LTD

⚠️ Moderate Risk

FEI: 3014531964 • Edmonton Lodon • UNITED KINGDOM

FEI

FEI Number

3014531964

📍

Location

Edmonton Lodon

🇬🇧
🏢

Address

Picketts Lock Lane, , Edmonton Lodon, , United Kingdom

Moderate Risk

FDA Import Risk Assessment

29.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
5
Unique Violations
6/7/2019
Latest Refusal
6/7/2019
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

1981×

COLOR LBLG

The color additive appears to not have its packaging and labeling in conformity with such requirements as issued under section 721.

3211×

LACKS N/C

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)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.

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.

4821×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

751×

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).

Refusal History

DateProductViolationsDivision
6/7/2019
64ABL99DISINFECTANT N.E.C.
335LACKS N/C
75UNAPPROVED
Division of Southeast Imports (DSEI)
6/7/2019
29AGT04SOFT DRINK, MIXED FRUIT FLAVORED, NONCARBONATED
321LACKS N/C
482NUTRIT LBL
Division of Southeast Imports (DSEI)
6/7/2019
53IG01DENTIFRICES (AEROSOL, LIQUID, TOOTHPASTES, TOOTHPOWDERS), WITHOUT FLUORIDE (ORAL HYGIENE PRODUCTS)
198COLOR LBLG
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is ABRA WHOLESALE LTD's FDA import refusal history?

ABRA WHOLESALE LTD (FEI: 3014531964) has 3 FDA import refusal record(s) in our database, spanning from 6/7/2019 to 6/7/2019.

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. ABRA WHOLESALE LTD's FEI number is 3014531964.

What types of violations has ABRA WHOLESALE LTD received?

ABRA WHOLESALE LTD 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 ABRA WHOLESALE LTD come from?

All FDA import refusal data for ABRA WHOLESALE 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.