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Synokem Pharmaecuticals Ltd

⚠️ High Risk

FEI: 3007485284 • Uttarakhand • INDIA

FEI

FEI Number

3007485284

📍

Location

Uttarakhand

🇮🇳

Country

INDIA
🏢

Address

Plot 35-36 Sec -6a Iie Sidcul Ra, , Uttarakhand, , India

High Risk

FDA Import Risk Assessment

62.5
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
5/26/2010
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
22.3×30%
Recency
98.0×20%
Frequency
1.9×10%
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
65JDA10DYDROGESTERONE (PROGESTIN)
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/8/2023
62CCY99ANTI-HYPERTENSIVE N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)
5/26/2010
65JDC38MIFEPRISTONE (PROGESTIN)
75UNAPPROVED
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Synokem Pharmaecuticals Ltd's FDA import refusal history?

Synokem Pharmaecuticals Ltd (FEI: 3007485284) has 3 FDA import refusal record(s) in our database, spanning from 5/26/2010 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. Synokem Pharmaecuticals Ltd's FEI number is 3007485284.

What types of violations has Synokem Pharmaecuticals Ltd received?

Synokem Pharmaecuticals Ltd 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 Synokem Pharmaecuticals Ltd come from?

All FDA import refusal data for Synokem Pharmaecuticals Ltd 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.