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MICRO LABS LIMITED

⚠️ Moderate Risk

FEI: 3018993628 • Thiruvandar Koil Pudu • INDIA

FEI

FEI Number

3018993628

📍

Location

Thiruvandar Koil Pudu

🇮🇳

Country

INDIA
🏢

Address

Rs No 63/3 &4 Thiruvan, , Thiruvandar Koil Pudu, , India

Moderate Risk

FDA Import Risk Assessment

43.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
10/17/2023
Latest Refusal
10/17/2023
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
11.2×30%
Recency
54.8×20%
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

1181×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

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
10/17/2023
60RCY18ORLISTAT/TETRAHYDROLIPSTATIN (ANOREXIC)
118NOT LISTED
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is MICRO LABS LIMITED's FDA import refusal history?

MICRO LABS LIMITED (FEI: 3018993628) has 1 FDA import refusal record(s) in our database, spanning from 10/17/2023 to 10/17/2023.

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 3018993628.

What types of violations has MICRO LABS LIMITED received?

MICRO LABS LIMITED 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 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.