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SUN HOUSE

⚠️ High Risk

FEI: 3012397513 • Mumbai, Maharashtra • INDIA

FEI

FEI Number

3012397513

📍

Location

Mumbai, Maharashtra

🇮🇳

Country

INDIA
🏢

Address

B 1 Cts No 201, Western India Industrial Estate, Mumbai, Maharashtra, India

High Risk

FDA Import Risk Assessment

57.7
LowModerateHighCritical

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

Statistics

4
Total Refusals
1
Unique Violations
12/12/2024
Latest Refusal
7/22/2021
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
25.9×30%
Recency
63.6×20%
Frequency
11.8×10%
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
12/12/2024
64BDC25HYDROCHLOROTHIAZIDE (DIURETIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
11/13/2024
56YYY99ANTIBIOTIC N.E.C.
75UNAPPROVED
Division of Northeast Imports (DNEI)
7/22/2021
61XDA51LEVOCETIRIZINE DIHYDROCHLORIDE
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/22/2021
61LDA13WARFARIN SODIUM (ANTI-COAGULANT)
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is SUN HOUSE's FDA import refusal history?

SUN HOUSE (FEI: 3012397513) has 4 FDA import refusal record(s) in our database, spanning from 7/22/2021 to 12/12/2024.

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. SUN HOUSE's FEI number is 3012397513.

What types of violations has SUN HOUSE received?

SUN HOUSE 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 SUN HOUSE come from?

All FDA import refusal data for SUN HOUSE 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.