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Gia-Mia Limited

⚠️ Moderate Risk

FEI: 3012156348 • Shenzhenshenzhen • CHINA

FEI

FEI Number

3012156348

📍

Location

Shenzhenshenzhen

🇨🇳

Country

CHINA
🏢

Address

Block CD Unit B22 Th Floor, 4 Taizi Rd, Shenzhenshenzhen, , China

Moderate Risk

FDA Import Risk Assessment

26.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
3/14/2016
Latest Refusal
3/14/2016
Earliest Refusal

Score Breakdown

Violation Severity
55.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

1181×

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).

2351×

NOT IMPACT

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

Refusal History

DateProductViolationsDivision
3/14/2016
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
235NOT IMPACT
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is Gia-Mia Limited's FDA import refusal history?

Gia-Mia Limited (FEI: 3012156348) has 1 FDA import refusal record(s) in our database, spanning from 3/14/2016 to 3/14/2016.

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. Gia-Mia Limited's FEI number is 3012156348.

What types of violations has Gia-Mia Limited received?

Gia-Mia Limited has been cited for 2 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 Gia-Mia Limited come from?

All FDA import refusal data for Gia-Mia 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.