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Joyce Taylor

⚠️ Moderate Risk

FEI: 3011026301 • Accra • GHANA

FEI

FEI Number

3011026301

📍

Location

Accra

🇬🇭

Country

GHANA
🏢

Address

Po Box 217 Ofankor, , Accra, , Ghana

Moderate Risk

FDA Import Risk Assessment

37.5
LowModerateHighCritical

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

Statistics

14
Total Refusals
8
Unique Violations
4/20/2015
Latest Refusal
3/31/2015
Earliest Refusal

Score Breakdown

Violation Severity
36.1×40%
Refusal Volume
43.6×30%
Recency
0.0×20%
Frequency
100.0×10%
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

32014×

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.

32111×

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.

32810×

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.

4733×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

2182×

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.

4822×

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.

621×

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).

831×

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.

Refusal History

DateProductViolationsDivision
4/20/2015
16AFH99FISH, N.E.C.
320LACKS FIRM
321LACKS N/C
328USUAL NAME
Division of Northeast Imports (DNEI)
4/20/2015
16AFH99FISH, N.E.C.
320LACKS FIRM
321LACKS N/C
328USUAL NAME
Division of Northeast Imports (DNEI)
4/20/2015
16AFH99FISH, N.E.C.
320LACKS FIRM
321LACKS N/C
328USUAL NAME
Division of Northeast Imports (DNEI)
4/20/2015
16AFH99FISH, N.E.C.
320LACKS FIRM
321LACKS N/C
328USUAL NAME
Division of Northeast Imports (DNEI)
4/20/2015
16AFH99FISH, N.E.C.
320LACKS FIRM
321LACKS N/C
328USUAL NAME
Division of Northeast Imports (DNEI)
3/31/2015
54FYT99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
320LACKS FIRM
473LABELING
Division of Northeast Imports (DNEI)
3/31/2015
16AEE73MACKEREL (ALL EXCEPT SCOMBEROMORUS SP, EG SPANISH OR KING SEE '22')
320LACKS FIRM
321LACKS N/C
482NUTRIT LBL
62NEEDS FCE
83NO PROCESS
Division of Northeast Imports (DNEI)
3/31/2015
23YGT99NUTS OR EDIBLE SEEDS NOT MENTIONED ELSEWHERE, N.E.C.
320LACKS FIRM
321LACKS N/C
328USUAL NAME
482NUTRIT LBL
Division of Northeast Imports (DNEI)
3/31/2015
25JGH99ROOT & TUBER VEGETABLE, N.E.C.
320LACKS FIRM
321LACKS N/C
328USUAL NAME
Division of Northeast Imports (DNEI)
3/31/2015
02AGH06RICE, WILD, WHOLE GRAIN
320LACKS FIRM
321LACKS N/C
328USUAL NAME
Division of Northeast Imports (DNEI)
3/31/2015
24AGH99BEANS, CORN, AND PEA, N.E.C. (VEGETABLE)
320LACKS FIRM
321LACKS N/C
328USUAL NAME
Division of Northeast Imports (DNEI)
3/31/2015
02GGH99FLOURS AND MEALS N.E.C.
320LACKS FIRM
321LACKS N/C
328USUAL NAME
Division of Northeast Imports (DNEI)
3/31/2015
54FYY99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
218LIST INGRE
320LACKS FIRM
473LABELING
Division of Northeast Imports (DNEI)
3/31/2015
54FYY99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
218LIST INGRE
320LACKS FIRM
473LABELING
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is Joyce Taylor's FDA import refusal history?

Joyce Taylor (FEI: 3011026301) has 14 FDA import refusal record(s) in our database, spanning from 3/31/2015 to 4/20/2015.

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. Joyce Taylor's FEI number is 3011026301.

What types of violations has Joyce Taylor received?

Joyce Taylor 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 Joyce Taylor come from?

All FDA import refusal data for Joyce Taylor 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.