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wrenco ltd

⚠️ Moderate Risk

FEI: 3009649043 • Accra, Greater Accra • GHANA

FEI

FEI Number

3009649043

📍

Location

Accra, Greater Accra

🇬🇭

Country

GHANA
🏢

Address

29 Kotoko Ave, , Accra, Greater Accra, Ghana

Moderate Risk

FDA Import Risk Assessment

42.2
LowModerateHighCritical

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

Statistics

9
Total Refusals
7
Unique Violations
10/2/2013
Latest Refusal
8/6/2013
Earliest Refusal

Score Breakdown

Violation Severity
55.3×40%
Refusal Volume
37.0×30%
Recency
0.0×20%
Frequency
90.0×10%
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

4824×

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.

3214×

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.

623×

NEEDS FCE

It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).

833×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

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.

2601×

FALSE

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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.

111×

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).

Refusal History

DateProductViolationsDivision
10/2/2013
02HHT01TAPIOCA STARCH PRODUCT
321LACKS N/C
482NUTRIT LBL
Division of Northeast Imports (DNEI)
10/2/2013
02HHT01TAPIOCA STARCH PRODUCT
321LACKS N/C
482NUTRIT LBL
Division of Northeast Imports (DNEI)
10/2/2013
02HHT01TAPIOCA STARCH PRODUCT
321LACKS N/C
482NUTRIT LBL
Division of Northeast Imports (DNEI)
10/2/2013
02HHT01TAPIOCA STARCH PRODUCT
321LACKS N/C
Division of Northeast Imports (DNEI)
10/2/2013
02HFT01TAPIOCA STARCH PRODUCT
260FALSE
328USUAL NAME
Division of Northeast Imports (DNEI)
10/2/2013
02HFT01TAPIOCA STARCH PRODUCT
11UNSAFE COL
482NUTRIT LBL
Division of Northeast Imports (DNEI)
8/21/2013
24KEI01EGG PLANT, WITH SAUCE
62NEEDS FCE
83NO PROCESS
Division of Northeast Imports (DNEI)
8/6/2013
16AEE45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
62NEEDS FCE
83NO PROCESS
Division of Northeast Imports (DNEI)
8/6/2013
16AEE45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
62NEEDS FCE
83NO PROCESS
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is wrenco ltd's FDA import refusal history?

wrenco ltd (FEI: 3009649043) has 9 FDA import refusal record(s) in our database, spanning from 8/6/2013 to 10/2/2013.

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. wrenco ltd's FEI number is 3009649043.

What types of violations has wrenco ltd received?

wrenco ltd has been cited for 7 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 wrenco ltd come from?

All FDA import refusal data for wrenco 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.