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Taizhou Hongfa Glasses Co., Ltd.

⚠️ Moderate Risk

FEI: 3008490214 • Taizhou, Zhejiang • CHINA

FEI

FEI Number

3008490214

📍

Location

Taizhou, Zhejiang

🇨🇳

Country

CHINA
🏢

Address

Duqiao Taizhou, , Taizhou, Zhejiang, China

Moderate Risk

FDA Import Risk Assessment

40.0
LowModerateHighCritical

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

Statistics

23
Total Refusals
6
Unique Violations
1/11/2021
Latest Refusal
1/14/2015
Earliest Refusal

Score Breakdown

Violation Severity
52.1×40%
Refusal Volume
51.1×30%
Recency
0.0×20%
Frequency
38.4×10%
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

23515×

NOT IMPACT

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

11812×

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).

32809×

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.

2316×

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.

3414×

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).

3331×

LACKS FIRM

The article is in package form and appears to not bear a label containing the name and place of business of the manufacturer, packer, or distributor.

Refusal History

DateProductViolationsDivision
1/11/2021
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
235NOT IMPACT
3280FRNMFGREG
341REGISTERED
Division of Southeast Imports (DSEI)
12/29/2017
86HQZFRAME, SPECTACLE
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
11/13/2017
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
231LENS CERT
235NOT IMPACT
3280FRNMFGREG
Division of Southeast Imports (DSEI)
8/23/2017
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
235NOT IMPACT
3280FRNMFGREG
Division of Northern Border Imports (DNBI)
6/19/2017
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
6/16/2017
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
235NOT IMPACT
3280FRNMFGREG
Division of Southeast Imports (DSEI)
6/13/2017
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
235NOT IMPACT
Division of Southeast Imports (DSEI)
6/1/2017
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
235NOT IMPACT
341REGISTERED
Division of Northern Border Imports (DNBI)
5/4/2017
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
235NOT IMPACT
3280FRNMFGREG
Division of Southeast Imports (DSEI)
3/22/2017
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
231LENS CERT
Division of Southeast Imports (DSEI)
12/6/2016
86HQZFRAME, SPECTACLE
235NOT IMPACT
Division of Southeast Imports (DSEI)
11/16/2016
86HQZFRAME, SPECTACLE
231LENS CERT
235NOT IMPACT
Division of West Coast Imports (DWCI)
10/17/2016
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
235NOT IMPACT
Division of Southeast Imports (DSEI)
9/28/2016
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
235NOT IMPACT
Seattle District Office (SEA-DO)
8/4/2016
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
231LENS CERT
235NOT IMPACT
341REGISTERED
Chicago District Office (CHI-DO)
6/10/2016
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
231LENS CERT
341REGISTERED
Los Angeles District Office (LOS-DO)
4/20/2016
86HOISPECTACLE, MAGNIFYING
235NOT IMPACT
Seattle District Office (SEA-DO)
4/20/2016
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
235NOT IMPACT
Seattle District Office (SEA-DO)
4/14/2016
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
3280FRNMFGREG
Seattle District Office (SEA-DO)
9/22/2015
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
3280FRNMFGREG
Cincinnati District Office (CIN-DO)
8/24/2015
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
333LACKS FIRM
Cincinnati District Office (CIN-DO)
6/30/2015
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
231LENS CERT
San Francisco District Office (SAN-DO)
1/14/2015
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
235NOT IMPACT
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Taizhou Hongfa Glasses Co., Ltd.'s FDA import refusal history?

Taizhou Hongfa Glasses Co., Ltd. (FEI: 3008490214) has 23 FDA import refusal record(s) in our database, spanning from 1/14/2015 to 1/11/2021.

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. Taizhou Hongfa Glasses Co., Ltd.'s FEI number is 3008490214.

What types of violations has Taizhou Hongfa Glasses Co., Ltd. received?

Taizhou Hongfa Glasses Co., Ltd. has been cited for 6 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 Taizhou Hongfa Glasses Co., Ltd. come from?

All FDA import refusal data for Taizhou Hongfa Glasses 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.