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AKUMS DRUGS AND PHARMACEUTICALS

⚠️ High Risk

FEI: 3012870049 • HARIDWAR • INDIA

FEI

FEI Number

3012870049

📍

Location

HARIDWAR

🇮🇳

Country

INDIA
🏢

Address

47-48 SECTOR 6A, LLE, S, , HARIDWAR, , India

High Risk

FDA Import Risk Assessment

61.8
LowModerateHighCritical

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

Statistics

4
Total Refusals
1
Unique Violations
10/14/2025
Latest Refusal
9/8/2023
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
25.9×30%
Recency
80.9×20%
Frequency
19.0×10%
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

754×

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
10/14/2025
66VDY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)
11/22/2024
65JDY17HALOPROGESTERONE (PROGESTIN)
75UNAPPROVED
Division of Southeast Imports (DSEI)
11/13/2024
66VDY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Northeast Imports (DNEI)
9/8/2023
64GCO07ESTRADIOL (ESTROGEN)
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is AKUMS DRUGS AND PHARMACEUTICALS's FDA import refusal history?

AKUMS DRUGS AND PHARMACEUTICALS (FEI: 3012870049) has 4 FDA import refusal record(s) in our database, spanning from 9/8/2023 to 10/14/2025.

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. AKUMS DRUGS AND PHARMACEUTICALS's FEI number is 3012870049.

What types of violations has AKUMS DRUGS AND PHARMACEUTICALS received?

AKUMS DRUGS AND PHARMACEUTICALS has been cited for 1 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 AKUMS DRUGS AND PHARMACEUTICALS come from?

All FDA import refusal data for AKUMS DRUGS AND PHARMACEUTICALS 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.