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Madhavi Desai

⚠️ Moderate Risk

FEI: 3003542822 • Maharastr • INDIA

FEI

FEI Number

3003542822

📍

Location

Maharastr

🇮🇳

Country

INDIA
🏢

Address

Sir Pochkanwala, , Maharastr, , India

Moderate Risk

FDA Import Risk Assessment

34.3
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

1
Total Refusals
2
Unique Violations
3/16/2002
Latest Refusal
3/16/2002
Earliest Refusal

Score Breakdown

Violation Severity
75.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

1791×

AGR RX

The article appears to be a prescription drug manufactured in the U.S. and offered for import by other than the manufacturer and reimportation does not appear to have been authorized by the Secretary for use in a medical emergency.

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
3/16/2002
61FDY54CIPROFLOXACIN (ANTI-BACTERIAL PART I) (NOT ANTIBIOTIC)
179AGR RX
75UNAPPROVED
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Madhavi Desai's FDA import refusal history?

Madhavi Desai (FEI: 3003542822) has 1 FDA import refusal record(s) in our database, spanning from 3/16/2002 to 3/16/2002.

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. Madhavi Desai's FEI number is 3003542822.

What types of violations has Madhavi Desai received?

Madhavi Desai 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 Madhavi Desai come from?

All FDA import refusal data for Madhavi Desai 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.