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Ever Eyewear Co., Ltd

⚠️ Moderate Risk

FEI: 3005925379 • Zhenjiang • CHINA

FEI

FEI Number

3005925379

📍

Location

Zhenjiang

🇨🇳

Country

CHINA
🏢

Address

P O Box 3018, Wenzhou, , Zhenjiang, , China

Moderate Risk

FDA Import Risk Assessment

37.4
LowModerateHighCritical

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

Statistics

20
Total Refusals
5
Unique Violations
3/16/2017
Latest Refusal
11/16/2011
Earliest Refusal

Score Breakdown

Violation Severity
47.4×40%
Refusal Volume
49.0×30%
Recency
0.0×20%
Frequency
37.5×10%
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

23513×

NOT IMPACT

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

328010×

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.

374110×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(o) in that it is being imported or offered for import into the United States, and the importer, owner, or consignee of such article did not, at the time of offering the article for import, submit to the Secretary a statement that identifies the registration under section 510(i) of the Act of each establishment that with respect to such article is required under such section to register with the Secretary.

1187×

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).

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).

Refusal History

DateProductViolationsDivision
3/16/2017
86HQZFRAME, SPECTACLE
3280FRNMFGREG
New Orleans District Office (NOL-DO)
11/18/2013
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
235NOT IMPACT
New Orleans District Office (NOL-DO)
11/12/2013
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
235NOT IMPACT
3741FRNMFGREG
New Orleans District Office (NOL-DO)
11/12/2013
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
235NOT IMPACT
3280FRNMFGREG
3741FRNMFGREG
New Orleans District Office (NOL-DO)
11/12/2013
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
235NOT IMPACT
3280FRNMFGREG
3741FRNMFGREG
New Orleans District Office (NOL-DO)
11/12/2013
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
235NOT IMPACT
3280FRNMFGREG
3741FRNMFGREG
New Orleans District Office (NOL-DO)
11/12/2013
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
235NOT IMPACT
3280FRNMFGREG
3741FRNMFGREG
New Orleans District Office (NOL-DO)
11/12/2013
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
235NOT IMPACT
3280FRNMFGREG
3741FRNMFGREG
New Orleans District Office (NOL-DO)
11/12/2013
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
235NOT IMPACT
3280FRNMFGREG
3741FRNMFGREG
New Orleans District Office (NOL-DO)
11/12/2013
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
235NOT IMPACT
3280FRNMFGREG
3741FRNMFGREG
New Orleans District Office (NOL-DO)
11/12/2013
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
235NOT IMPACT
3280FRNMFGREG
3741FRNMFGREG
New Orleans District Office (NOL-DO)
11/12/2013
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
235NOT IMPACT
3280FRNMFGREG
3741FRNMFGREG
New Orleans District Office (NOL-DO)
6/14/2013
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
235NOT IMPACT
341REGISTERED
New Orleans District Office (NOL-DO)
4/20/2012
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
New Orleans District Office (NOL-DO)
2/17/2012
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
New Orleans District Office (NOL-DO)
2/17/2012
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
New Orleans District Office (NOL-DO)
2/17/2012
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
New Orleans District Office (NOL-DO)
2/17/2012
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
New Orleans District Office (NOL-DO)
2/17/2012
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
New Orleans District Office (NOL-DO)
11/16/2011
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
235NOT IMPACT
341REGISTERED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Ever Eyewear Co., Ltd's FDA import refusal history?

Ever Eyewear Co., Ltd (FEI: 3005925379) has 20 FDA import refusal record(s) in our database, spanning from 11/16/2011 to 3/16/2017.

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. Ever Eyewear Co., Ltd's FEI number is 3005925379.

What types of violations has Ever Eyewear Co., Ltd received?

Ever Eyewear Co., Ltd 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 Ever Eyewear Co., Ltd come from?

All FDA import refusal data for Ever Eyewear Co., Ltd 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.