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Prime Food Distributors

⚠️ Moderate Risk

FEI: 3023273683 • Kartah, AF-HER • AFGHANISTAN

FEI

FEI Number

3023273683

📍

Location

Kartah, AF-HER

🇦🇫
🏢

Address

Charahi Zaman Jan, House#51, , Kartah, AF-HER, Afghanistan

Moderate Risk

FDA Import Risk Assessment

45.7
LowModerateHighCritical

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

Statistics

6
Total Refusals
4
Unique Violations
11/10/2022
Latest Refusal
11/10/2022
Earliest Refusal

Score Breakdown

Violation Severity
57.5×40%
Refusal Volume
31.3×30%
Recency
36.6×20%
Frequency
60.0×10%
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

3206×

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.

4826×

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.

626×

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).

836×

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
11/10/2022
38MEN99BROTH, N.E.C. (MEAT AND/OR VEGETABLE STOCK)
320LACKS FIRM
482NUTRIT LBL
62NEEDS FCE
83NO PROCESS
Division of Northern Border Imports (DNBI)
11/10/2022
24VEN11CELERY, WITH SAUCE
320LACKS FIRM
482NUTRIT LBL
62NEEDS FCE
83NO PROCESS
Division of Northern Border Imports (DNBI)
11/10/2022
18YEN99VEGETABLE PROTEIN PRODUCTS NOT ELSEWHERE MENTIONED, N.E.C.
320LACKS FIRM
482NUTRIT LBL
62NEEDS FCE
83NO PROCESS
Division of Northern Border Imports (DNBI)
11/10/2022
37DEN99STEW, N.E.C.
320LACKS FIRM
482NUTRIT LBL
62NEEDS FCE
83NO PROCESS
Division of Northern Border Imports (DNBI)
11/10/2022
24KEN01EGG PLANT, WITH SAUCE
320LACKS FIRM
482NUTRIT LBL
62NEEDS FCE
83NO PROCESS
Division of Northern Border Imports (DNBI)
11/10/2022
37DEN99STEW, N.E.C.
320LACKS FIRM
482NUTRIT LBL
62NEEDS FCE
83NO PROCESS
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is Prime Food Distributors's FDA import refusal history?

Prime Food Distributors (FEI: 3023273683) has 6 FDA import refusal record(s) in our database, spanning from 11/10/2022 to 11/10/2022.

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. Prime Food Distributors's FEI number is 3023273683.

What types of violations has Prime Food Distributors received?

Prime Food Distributors 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 Prime Food Distributors come from?

All FDA import refusal data for Prime Food Distributors 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.