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Unison Pharmaceuticals

⚠️ High Risk

FEI: 3009102764 • Ahmedabad • INDIA

FEI

FEI Number

3009102764

📍

Location

Ahmedabad

🇮🇳

Country

INDIA
🏢

Address

Steel Town Moraiya Ta Sanand, , Ahmedabad, , India

High Risk

FDA Import Risk Assessment

62.6
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
1/22/2026
Latest Refusal
1/27/2016
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
22.3×30%
Recency
98.0×20%
Frequency
3.0×10%
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

753×

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
1/22/2026
60LDY01ACETAMINOPHEN (ANALGESIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
8/31/2017
66VCY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)
1/27/2016
62OCA14AMLODIPINE BESYLATE (ANTI-HYPERTENSIVE, PART II)
75UNAPPROVED
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is Unison Pharmaceuticals's FDA import refusal history?

Unison Pharmaceuticals (FEI: 3009102764) has 3 FDA import refusal record(s) in our database, spanning from 1/27/2016 to 1/22/2026.

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. Unison Pharmaceuticals's FEI number is 3009102764.

What types of violations has Unison Pharmaceuticals received?

Unison 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 Unison Pharmaceuticals come from?

All FDA import refusal data for Unison 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.