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Mc Lyrit Enterprise

⚠️ Moderate Risk

FEI: 3008290691 • Bantama • GHANA

FEI

FEI Number

3008290691

📍

Location

Bantama

🇬🇭

Country

GHANA
🏢

Address

P.O. Box Ba 255 Bantamaashanti Region, , Bantama, , Ghana

Moderate Risk

FDA Import Risk Assessment

37.3
LowModerateHighCritical

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

Statistics

5
Total Refusals
4
Unique Violations
2/16/2012
Latest Refusal
5/9/2011
Earliest Refusal

Score Breakdown

Violation Severity
59.0×40%
Refusal Volume
28.8×30%
Recency
0.0×20%
Frequency
50.0×10%
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

2184×

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.

3064×

INSANITARY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.

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.

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.

Refusal History

DateProductViolationsDivision
2/16/2012
03FGT06SALTED CRACKERS
321LACKS N/C
482NUTRIT LBL
New York District Office (NYK-DO)
5/9/2011
28EFT03FIVE SPICE MIX, WITHOUT SALT
218LIST INGRE
306INSANITARY
New York District Office (NYK-DO)
5/9/2011
28BFH54PEPPER, BLACK, GROUND, CRACKED (SPICE)
218LIST INGRE
306INSANITARY
New York District Office (NYK-DO)
5/9/2011
05YFH99CEREAL PREPARATIONS NOT ELSEWHERE MENTIONED, N.E.C.
218LIST INGRE
306INSANITARY
New York District Office (NYK-DO)
5/9/2011
25JFH16CASSAVA (ROOT AND TUBER VEGETABLE)
218LIST INGRE
306INSANITARY
New York District Office (NYK-DO)

Frequently Asked Questions

What is Mc Lyrit Enterprise's FDA import refusal history?

Mc Lyrit Enterprise (FEI: 3008290691) has 5 FDA import refusal record(s) in our database, spanning from 5/9/2011 to 2/16/2012.

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. Mc Lyrit Enterprise's FEI number is 3008290691.

What types of violations has Mc Lyrit Enterprise received?

Mc Lyrit 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 Mc Lyrit Enterprise come from?

All FDA import refusal data for Mc Lyrit 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.