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Hongkong Optone Te

⚠️ Moderate Risk

FEI: 3012160805 • Shenzhen City • CHINA

FEI

FEI Number

3012160805

📍

Location

Shenzhen City

🇨🇳

Country

CHINA
🏢

Address

Shi Yan Town, , Shenzhen City, , China

Moderate Risk

FDA Import Risk Assessment

40.9
LowModerateHighCritical

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

Statistics

11
Total Refusals
4
Unique Violations
3/25/2016
Latest Refusal
3/25/2016
Earliest Refusal

Score Breakdown

Violation Severity
47.2×40%
Refusal Volume
40.0×30%
Recency
0.0×20%
Frequency
100.0×10%
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

11811×

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).

23511×

NOT IMPACT

The article appears to not have impact-resistant lenses in accordance with 21 CFR 801.410.

34111×

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).

32806×

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
3/25/2016
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
235NOT IMPACT
3280FRNMFGREG
341REGISTERED
Division of West Coast Imports (DWCI)
3/25/2016
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
235NOT IMPACT
3280FRNMFGREG
341REGISTERED
Division of West Coast Imports (DWCI)
3/25/2016
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
235NOT IMPACT
3280FRNMFGREG
341REGISTERED
Division of West Coast Imports (DWCI)
3/25/2016
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
235NOT IMPACT
3280FRNMFGREG
341REGISTERED
Division of West Coast Imports (DWCI)
3/25/2016
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
235NOT IMPACT
3280FRNMFGREG
341REGISTERED
Division of West Coast Imports (DWCI)
3/25/2016
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
235NOT IMPACT
3280FRNMFGREG
341REGISTERED
Division of West Coast Imports (DWCI)
3/25/2016
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
235NOT IMPACT
341REGISTERED
Division of West Coast Imports (DWCI)
3/25/2016
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
235NOT IMPACT
341REGISTERED
Division of West Coast Imports (DWCI)
3/25/2016
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
235NOT IMPACT
341REGISTERED
Division of West Coast Imports (DWCI)
3/25/2016
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
235NOT IMPACT
341REGISTERED
Division of West Coast Imports (DWCI)
3/25/2016
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
235NOT IMPACT
341REGISTERED
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is Hongkong Optone Te's FDA import refusal history?

Hongkong Optone Te (FEI: 3012160805) has 11 FDA import refusal record(s) in our database, spanning from 3/25/2016 to 3/25/2016.

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. Hongkong Optone Te's FEI number is 3012160805.

What types of violations has Hongkong Optone Te received?

Hongkong Optone Te has been cited for 4 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 Hongkong Optone Te come from?

All FDA import refusal data for Hongkong Optone Te 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.