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Argent Optical Manufactory Limited

⚠️ Moderate Risk

FEI: 3003117010 • Long Gang Area Shenzhen • CHINA

FEI

FEI Number

3003117010

📍

Location

Long Gang Area Shenzhen

🇨🇳

Country

CHINA
🏢

Address

Huang Ge Keng, Long Cheng, , Long Gang Area Shenzhen, , China

Moderate Risk

FDA Import Risk Assessment

33.6
LowModerateHighCritical

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

Statistics

11
Total Refusals
4
Unique Violations
3/29/2018
Latest Refusal
6/24/2011
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
40.0×30%
Recency
0.0×20%
Frequency
16.3×10%
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

1186×

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).

2313×

LENS CERT

The lenses are declared by accompanying certificate to meet the requirements for impact-resistant lenses in 21 CFR 801.410 but does not appear to be impact-resistant.

3412×

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).

2351×

NOT IMPACT

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

Refusal History

DateProductViolationsDivision
3/29/2018
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
Division of Southeast Imports (DSEI)
8/16/2016
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
Division of Southeast Imports (DSEI)
8/16/2016
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
Division of Southeast Imports (DSEI)
3/17/2016
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
Florida District Office (FLA-DO)
3/17/2016
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
Florida District Office (FLA-DO)
12/3/2015
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
341REGISTERED
Division of Southeast Imports (DSEI)
1/7/2014
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
341REGISTERED
New York District Office (NYK-DO)
1/24/2013
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
231LENS CERT
San Francisco District Office (SAN-DO)
7/19/2012
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
231LENS CERT
San Francisco District Office (SAN-DO)
7/19/2011
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
231LENS CERT
San Francisco District Office (SAN-DO)
6/24/2011
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
235NOT IMPACT
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Argent Optical Manufactory Limited's FDA import refusal history?

Argent Optical Manufactory Limited (FEI: 3003117010) has 11 FDA import refusal record(s) in our database, spanning from 6/24/2011 to 3/29/2018.

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. Argent Optical Manufactory Limited's FEI number is 3003117010.

What types of violations has Argent Optical Manufactory Limited received?

Argent Optical Manufactory Limited 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 Argent Optical Manufactory Limited come from?

All FDA import refusal data for Argent Optical Manufactory 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.