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Micro Labs Limited

⚠️ High Risk

FEI: 3013225177 • Bangalore, Karnataka • INDIA

FEI

FEI Number

3013225177

📍

Location

Bangalore, Karnataka

🇮🇳

Country

INDIA
🏢

Address

UNIT II 67/68A, 3RD Phase, Peenya Industrial Park, , Bangalore, Karnataka, India

High Risk

FDA Import Risk Assessment

56.0
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
12/3/2024
Latest Refusal
3/1/2021
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
22.3×30%
Recency
62.8×20%
Frequency
8.0×10%
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
12/3/2024
62SDY03AZELAIC ACID (ANTI-SEBORRHEIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
4/12/2021
66NCY07OXCARBAZEPINE (TRANQUILIZER (ANTI-PSYCHOTIC) - PART II)
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/1/2021
62OCB14AMLODIPINE BESYLATE (ANTI-HYPERTENSIVE, PART II)
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Micro Labs Limited's FDA import refusal history?

Micro Labs Limited (FEI: 3013225177) has 3 FDA import refusal record(s) in our database, spanning from 3/1/2021 to 12/3/2024.

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. Micro Labs Limited's FEI number is 3013225177.

What types of violations has Micro Labs Limited received?

Micro Labs Limited 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 Micro Labs Limited come from?

All FDA import refusal data for Micro Labs Limited 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.