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OTICA MEDITRONIX CO

⚠️ Moderate Risk

FEI: 3032006708 • Vadodara, Gujarat • INDIA

FEI

FEI Number

3032006708

📍

Location

Vadodara, Gujarat

🇮🇳

Country

INDIA
🏢

Address

B - 16 Behind Pani Tanki, , Vadodara, Gujarat, India

Moderate Risk

FDA Import Risk Assessment

42.8
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
2/13/2025
Latest Refusal
1/13/2025
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
17.7×30%
Recency
77.6×20%
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

1182×

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).

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

Refusal History

DateProductViolationsDivision
2/13/2025
80KYTLIGHT, EXAMINATION, MEDICAL, BATTERY POWERED
118NOT LISTED
Division of Southeast Imports (DSEI)
1/13/2025
80KYTLIGHT, EXAMINATION, MEDICAL, BATTERY POWERED
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is OTICA MEDITRONIX CO's FDA import refusal history?

OTICA MEDITRONIX CO (FEI: 3032006708) has 2 FDA import refusal record(s) in our database, spanning from 1/13/2025 to 2/13/2025.

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. OTICA MEDITRONIX CO's FEI number is 3032006708.

What types of violations has OTICA MEDITRONIX CO received?

OTICA MEDITRONIX CO 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 OTICA MEDITRONIX CO come from?

All FDA import refusal data for OTICA MEDITRONIX CO 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.