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Zhejiang Ouhai International

⚠️ Moderate Risk

FEI: 3008154091 • Whenzhou • CHINA

FEI

FEI Number

3008154091

📍

Location

Whenzhou

🇨🇳

Country

CHINA
🏢

Address

Wenzhou Rd 6th-7th Fl Bldg B, , Whenzhou, , China

Moderate Risk

FDA Import Risk Assessment

26.8
LowModerateHighCritical

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

Statistics

3
Total Refusals
4
Unique Violations
8/8/2014
Latest Refusal
9/17/2012
Earliest Refusal

Score Breakdown

Violation Severity
46.3×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
15.9×10%
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

1183×

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).

32802×

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.

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).

2311×

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.

Refusal History

DateProductViolationsDivision
8/8/2014
86HQZFRAME, SPECTACLE
118NOT LISTED
3280FRNMFGREG
341REGISTERED
Seattle District Office (SEA-DO)
8/8/2014
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
3280FRNMFGREG
341REGISTERED
Seattle District Office (SEA-DO)
9/17/2012
86HOISPECTACLE, MAGNIFYING
118NOT LISTED
231LENS CERT
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is Zhejiang Ouhai International's FDA import refusal history?

Zhejiang Ouhai International (FEI: 3008154091) has 3 FDA import refusal record(s) in our database, spanning from 9/17/2012 to 8/8/2014.

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. Zhejiang Ouhai International's FEI number is 3008154091.

What types of violations has Zhejiang Ouhai International received?

Zhejiang Ouhai International 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 Zhejiang Ouhai International come from?

All FDA import refusal data for Zhejiang Ouhai International 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.