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Crystal Field Ltd

⚠️ Moderate Risk

FEI: 3002190850 • Sha Tin, New Territories • HONG KONG

FEI

FEI Number

3002190850

📍

Location

Sha Tin, New Territories

🇭🇰

Country

HONG KONG
🏢

Address

16/F, 16/Flat, Goldfield Industrial Centre; 1 Sui Wo Road, Sha Tin, New Territories, Hong Kong

Moderate Risk

FDA Import Risk Assessment

31.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
6
Unique Violations
5/9/2003
Latest Refusal
12/7/2001
Earliest Refusal

Score Breakdown

Violation Severity
61.4×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
14.1×10%
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

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).

1171×

DANGEROUS

The article appears to be dangerous to health when used in the dosage or manner, or with the frequency or duration, prescribed, recommended, or suggested in the labeling thereof.

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).

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

23801×

NO PMA/PDP

The article appears to be a class III dev.w/o an approved applic. for premarket approval, and/or a notice of completion of product development protocol filed per section 515(b) or exempt per sect.520(g)(1).

5081×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

Refusal History

DateProductViolationsDivision
5/9/2003
84HCCDEVICE, BIOFEEDBACK
118NOT LISTED
341REGISTERED
Seattle District Office (SEA-DO)
12/7/2001
89LYGMASSAGER, THERAPEUTIC, MANUAL
117DANGEROUS
16DIRECTIONS
2380NO PMA/PDP
341REGISTERED
508NO 510(K)
San Francisco District Office (SAN-DO)

Frequently Asked Questions

What is Crystal Field Ltd's FDA import refusal history?

Crystal Field Ltd (FEI: 3002190850) has 2 FDA import refusal record(s) in our database, spanning from 12/7/2001 to 5/9/2003.

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. Crystal Field Ltd's FEI number is 3002190850.

What types of violations has Crystal Field Ltd received?

Crystal Field 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 Crystal Field Ltd come from?

All FDA import refusal data for Crystal Field 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.