ImportRefusal LogoImportRefusal

Nasem Product Enterprises

⚠️ Moderate Risk

FEI: 3001616005 • Accra • GHANA

FEI

FEI Number

3001616005

📍

Location

Accra

🇬🇭

Country

GHANA
🏢

Address

Po Box 10418, , Accra, , Ghana

Moderate Risk

FDA Import Risk Assessment

48.8
LowModerateHighCritical

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

Statistics

6
Total Refusals
5
Unique Violations
6/10/2003
Latest Refusal
11/30/2001
Earliest Refusal

Score Breakdown

Violation Severity
88.8×40%
Refusal Volume
31.3×30%
Recency
0.0×20%
Frequency
39.3×10%
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

2493×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

92×

SALMONELLA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.

3191×

WRONG IDEN

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 as defined in section 403(b) of the FD&C Act. The article appears to be offered for sale under the name of another food.

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
6/10/2003
16SYH12COD, COLD SMOKED, FISH
249FILTHY
319WRONG IDEN
New York District Office (NYK-DO)
11/19/2002
24KCT01EGG PLANT, WITH SAUCE
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
9/19/2002
16IFN12COD, HOT SMOKED, FISH
249FILTHY
New York District Office (NYK-DO)
5/8/2002
16MHD15SNAILS, TERRESTRIAL (E.G., LAND), OTHER AQUATIC SPECIES
9SALMONELLA
New York District Office (NYK-DO)
3/25/2002
16IFN12COD, HOT SMOKED, FISH
249FILTHY
New York District Office (NYK-DO)
11/30/2001
16MFT03SQUID, OTHER AQUATIC SPECIES
9SALMONELLA
Baltimore District Office (BLT-DO)

Frequently Asked Questions

What is Nasem Product Enterprises's FDA import refusal history?

Nasem Product Enterprises (FEI: 3001616005) has 6 FDA import refusal record(s) in our database, spanning from 11/30/2001 to 6/10/2003.

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. Nasem Product Enterprises's FEI number is 3001616005.

What types of violations has Nasem Product Enterprises received?

Nasem Product Enterprises 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 Nasem Product Enterprises come from?

All FDA import refusal data for Nasem Product Enterprises 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.