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EXCELLENT HI CARE

⚠️ High Risk

FEI: 3013750452 • Chennai • INDIA

FEI

FEI Number

3013750452

📍

Location

Chennai

🇮🇳

Country

INDIA
🏢

Address

New No 25 /2 Anna Stree, , Chennai, , India

High Risk

FDA Import Risk Assessment

51.0
LowModerateHighCritical

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

Statistics

4
Total Refusals
5
Unique Violations
1/22/2026
Latest Refusal
4/13/2021
Earliest Refusal

Score Breakdown

Violation Severity
56.9×40%
Refusal Volume
25.9×30%
Recency
97.9×20%
Frequency
8.4×10%
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

1184×

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).

32804×

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.

2373×

NO PMA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).

3411×

REGISTERED

It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).

5081×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

Refusal History

DateProductViolationsDivision
1/22/2026
86HQLLENS, INTRAOCULAR
118NOT LISTED
237NO PMA
3280FRNMFGREG
Division of Southeast Imports (DSEI)
11/21/2025
86HQLLENS, INTRAOCULAR
118NOT LISTED
237NO PMA
3280FRNMFGREG
Division of Southeast Imports (DSEI)
4/12/2024
86MVNLENS, CONTACT (DISPOSABLE)
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
4/13/2021
86HQLLENS, INTRAOCULAR
118NOT LISTED
237NO PMA
3280FRNMFGREG
341REGISTERED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is EXCELLENT HI CARE's FDA import refusal history?

EXCELLENT HI CARE (FEI: 3013750452) has 4 FDA import refusal record(s) in our database, spanning from 4/13/2021 to 1/22/2026.

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. EXCELLENT HI CARE's FEI number is 3013750452.

What types of violations has EXCELLENT HI CARE received?

EXCELLENT HI CARE has been cited for 5 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 EXCELLENT HI CARE come from?

All FDA import refusal data for EXCELLENT HI CARE 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.