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MAC IMPEX

⚠️ High Risk

FEI: 3017835705 • Navi Mumbai • INDIA

FEI

FEI Number

3017835705

📍

Location

Navi Mumbai

🇮🇳

Country

INDIA
🏢

Address

Plot No. C-147, TTC Industrial Area, MIDC, Opp . Bhawkaleshwar Mandir, Pawne, Navi Mumbai, , India

High Risk

FDA Import Risk Assessment

55.7
LowModerateHighCritical

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

Statistics

7
Total Refusals
6
Unique Violations
11/4/2024
Latest Refusal
7/21/2021
Earliest Refusal

Score Breakdown

Violation Severity
77.8×40%
Refusal Volume
33.5×30%
Recency
62.0×20%
Frequency
21.3×10%
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

2494×

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.

111×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

2181×

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.

4741×

COSMETLBLG

It appears the label does not bear the common or usual name of the cosmetic.

4751×

COSMETLBLG

It appears that the cosmetic consists of two or more ingredients and the label does not list the common or usual name of each ingredient.

751×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

Refusal History

DateProductViolationsDivision
11/4/2024
29BET50SOFT DRINK, COLA, CARBONATED
218LIST INGRE
Division of Northern Border Imports (DNBI)
11/4/2024
29BET11SODA WATER WITH FRUIT FLAVOR, CARBONATED
11UNSAFE COL
Division of Northern Border Imports (DNBI)
10/8/2024
53EH99OTHER HAIR PREPARATIONS, NON-COLORING), N.E.C.
474COSMETLBLG
475COSMETLBLG
75UNAPPROVED
Division of Northeast Imports (DNEI)
7/21/2021
28AGT54PEPPER,BLACK, WHOLE (SPICE)
249FILTHY
Division of Northeast Imports (DNEI)
7/21/2021
28AGT54PEPPER,BLACK, WHOLE (SPICE)
249FILTHY
Division of Northeast Imports (DNEI)
7/21/2021
28BGT54PEPPER, BLACK, GROUND, CRACKED (SPICE)
249FILTHY
Division of Northeast Imports (DNEI)
7/21/2021
28BGT54PEPPER, BLACK, GROUND, CRACKED (SPICE)
249FILTHY
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is MAC IMPEX's FDA import refusal history?

MAC IMPEX (FEI: 3017835705) has 7 FDA import refusal record(s) in our database, spanning from 7/21/2021 to 11/4/2024.

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. MAC IMPEX's FEI number is 3017835705.

What types of violations has MAC IMPEX received?

MAC IMPEX has been cited for 6 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 MAC IMPEX come from?

All FDA import refusal data for MAC IMPEX 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.