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VINAYAK PHARMA CHEM EQUIPMENT

⚠️ High Risk

FEI: 3031153132 • Haridwar • INDIA

FEI

FEI Number

3031153132

📍

Location

Haridwar

🇮🇳

Country

INDIA
🏢

Address

Plot No 47 56 Sector 18, , Haridwar, , India

High Risk

FDA Import Risk Assessment

52.4
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
1/16/2025
Latest Refusal
9/3/2024
Earliest Refusal

Score Breakdown

Violation Severity
75.0×40%
Refusal Volume
17.7×30%
Recency
75.3×20%
Frequency
20.0×10%
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

22801×

DIRSEXMPT

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a drug within the meaning of Section 201(g) and it lacks adequate directions for use.

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
1/16/2025
53LH03FACE,BODY,AND HAND (EXCLUDING SHAVING PREPARATIONS) (SKIN CARE PREPARATIONS)
2280DIRSEXMPT
Division of Northeast Imports (DNEI)
9/3/2024
66VBR99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is VINAYAK PHARMA CHEM EQUIPMENT's FDA import refusal history?

VINAYAK PHARMA CHEM EQUIPMENT (FEI: 3031153132) has 2 FDA import refusal record(s) in our database, spanning from 9/3/2024 to 1/16/2025.

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. VINAYAK PHARMA CHEM EQUIPMENT's FEI number is 3031153132.

What types of violations has VINAYAK PHARMA CHEM EQUIPMENT received?

VINAYAK PHARMA CHEM EQUIPMENT has been cited for 2 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 VINAYAK PHARMA CHEM EQUIPMENT come from?

All FDA import refusal data for VINAYAK PHARMA CHEM EQUIPMENT 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.