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TAYAAKO ENTERPRISE

⚠️ Moderate Risk

FEI: 3013022972 • Accra • GHANA

FEI

FEI Number

3013022972

📍

Location

Accra

🇬🇭

Country

GHANA
🏢

Address

217 P Box, , Accra, , Ghana

Moderate Risk

FDA Import Risk Assessment

26.8
LowModerateHighCritical

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

Statistics

5
Total Refusals
4
Unique Violations
9/8/2017
Latest Refusal
11/5/2007
Earliest Refusal

Score Breakdown

Violation Severity
44.0×40%
Refusal Volume
28.8×30%
Recency
0.0×20%
Frequency
5.1×10%
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

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.

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.

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
9/8/2017
25JFT23TARO, DASHEEN (ROOT & TUBER VEGETABLE)
321LACKS N/C
482NUTRIT LBL
Division of Northeast Imports (DNEI)
3/14/2014
02BGT01CORN, BOLTED MEAL OR FLOUR
321LACKS N/C
482NUTRIT LBL
Division of Northeast Imports (DNEI)
3/14/2014
02GGT99FLOURS AND MEALS N.E.C.
321LACKS N/C
482NUTRIT LBL
Division of Northeast Imports (DNEI)
3/14/2014
02BGT01CORN, BOLTED MEAL OR FLOUR
321LACKS N/C
482NUTRIT LBL
Division of Northeast Imports (DNEI)
11/5/2007
16AET33SARDINES (BRISLING, SPRATS, PILCHARDS, ETC.)
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)

Frequently Asked Questions

What is TAYAAKO ENTERPRISE's FDA import refusal history?

TAYAAKO ENTERPRISE (FEI: 3013022972) has 5 FDA import refusal record(s) in our database, spanning from 11/5/2007 to 9/8/2017.

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. TAYAAKO ENTERPRISE's FEI number is 3013022972.

What types of violations has TAYAAKO ENTERPRISE received?

TAYAAKO ENTERPRISE has been cited for 4 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 TAYAAKO ENTERPRISE come from?

All FDA import refusal data for TAYAAKO ENTERPRISE 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.