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MR PHARMA

⚠️ Moderate Risk

FEI: 3025123240 • Hira Garh, Punjab • INDIA

FEI

FEI Number

3025123240

📍

Location

Hira Garh, Punjab

🇮🇳

Country

INDIA
🏢

Address

1 New Rose Colony, Rajpura Road; Gali N0, Hira Garh, Punjab, India

Moderate Risk

FDA Import Risk Assessment

38.0
LowModerateHighCritical

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

Statistics

2
Total Refusals
3
Unique Violations
5/27/2025
Latest Refusal
10/10/2023
Earliest Refusal

Score Breakdown

Violation Severity
42.5×40%
Refusal Volume
17.7×30%
Recency
72.5×20%
Frequency
12.3×10%
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

4822×

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.

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.

38631×

PLANT PART

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(s)(2)(C) of the FD&C Act in that the supplement contains an herb or other botanical described in section 201(ff)(1)(C), and the label or labeling of the supplement fails to identify any part of the plant from which the ingredient is derived.

Refusal History

DateProductViolationsDivision
5/27/2025
54FCT99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
482NUTRIT LBL
Division of Southeast Imports (DSEI)
10/10/2023
54FCT99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
218LIST INGRE
3863PLANT PART
482NUTRIT LBL
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is MR PHARMA's FDA import refusal history?

MR PHARMA (FEI: 3025123240) has 2 FDA import refusal record(s) in our database, spanning from 10/10/2023 to 5/27/2025.

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. MR PHARMA's FEI number is 3025123240.

What types of violations has MR PHARMA received?

MR PHARMA has been cited for 3 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 MR PHARMA come from?

All FDA import refusal data for MR PHARMA 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.