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PAN FOODS

⚠️ High Risk

FEI: 3021810885 • Panipat • INDIA

FEI

FEI Number

3021810885

📍

Location

Panipat

🇮🇳

Country

INDIA
🏢

Address

G T Road, , Panipat, , India

High Risk

FDA Import Risk Assessment

52.5
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

6
Total Refusals
5
Unique Violations
8/27/2024
Latest Refusal
7/12/2023
Earliest Refusal

Score Breakdown

Violation Severity
65.3×40%
Refusal Volume
31.3×30%
Recency
58.1×20%
Frequency
53.2×10%
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

625×

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).

835×

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.

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.

3212×

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
8/27/2024
27YCT03CHUTNEY
218LIST INGRE
321LACKS N/C
62NEEDS FCE
83NO PROCESS
Division of Northeast Imports (DNEI)
6/17/2024
37JCY99SAUCES, N.E.C.
218LIST INGRE
321LACKS N/C
482NUTRIT LBL
Division of Northern Border Imports (DNBI)
7/12/2023
27YCY03CHUTNEY
62NEEDS FCE
83NO PROCESS
Division of West Coast Imports (DWCI)
7/12/2023
37JCY99SAUCES, N.E.C.
62NEEDS FCE
83NO PROCESS
Division of West Coast Imports (DWCI)
7/12/2023
27YCI03CHUTNEY
62NEEDS FCE
83NO PROCESS
Division of West Coast Imports (DWCI)
7/12/2023
37JCI03CHILI SAUCE
62NEEDS FCE
83NO PROCESS
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is PAN FOODS's FDA import refusal history?

PAN FOODS (FEI: 3021810885) has 6 FDA import refusal record(s) in our database, spanning from 7/12/2023 to 8/27/2024.

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. PAN FOODS's FEI number is 3021810885.

What types of violations has PAN FOODS received?

PAN FOODS 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 PAN FOODS come from?

All FDA import refusal data for PAN FOODS 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.