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Uniqso Holdings Sdn Bhd

⚠️ Moderate Risk

FEI: 3011990635 • Cheras, Selangor • MALAYSIA

FEI

FEI Number

3011990635

📍

Location

Cheras, Selangor

🇲🇾

Country

MALAYSIA
🏢

Address

Jalan Balakong Batu, 1/2, Cheras, Selangor, Malaysia

Moderate Risk

FDA Import Risk Assessment

33.5
LowModerateHighCritical

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

Statistics

8
Total Refusals
7
Unique Violations
8/24/2020
Latest Refusal
2/2/2016
Earliest Refusal

Score Breakdown

Violation Severity
52.9×40%
Refusal Volume
35.3×30%
Recency
0.0×20%
Frequency
17.5×10%
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

32808×

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.

1188×

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).

3338×

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.

5088×

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.

166×

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.

24802×

RXPERSONAL

The article appears to be a device which requires a prescription from your doctor.

842×

RX DEVICE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a prescription device that appears to not feature a prescription device legend as required by 21 CFR 801.109.

Refusal History

DateProductViolationsDivision
8/24/2020
86HQDLENS, CONTACT (OTHER MATERIAL) - DAILY
118NOT LISTED
2480RXPERSONAL
3280FRNMFGREG
333LACKS FIRM
508NO 510(K)
Division of Southeast Imports (DSEI)
8/24/2020
86HQDLENS, CONTACT (OTHER MATERIAL) - DAILY
118NOT LISTED
2480RXPERSONAL
3280FRNMFGREG
333LACKS FIRM
508NO 510(K)
Division of Southeast Imports (DSEI)
2/8/2016
86LPLLENSES, SOFT CONTACT, DAILY WEAR
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
333LACKS FIRM
508NO 510(K)
84RX DEVICE
Seattle District Office (SEA-DO)
2/3/2016
86NICLENS, CONTACT, FOR READING DISCOMFORT
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
333LACKS FIRM
508NO 510(K)
84RX DEVICE
Seattle District Office (SEA-DO)
2/2/2016
86LPLLENSES, SOFT CONTACT, DAILY WEAR
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
333LACKS FIRM
508NO 510(K)
Seattle District Office (SEA-DO)
2/2/2016
86LPLLENSES, SOFT CONTACT, DAILY WEAR
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
333LACKS FIRM
508NO 510(K)
Seattle District Office (SEA-DO)
2/2/2016
86NICLENS, CONTACT, FOR READING DISCOMFORT
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
333LACKS FIRM
508NO 510(K)
Seattle District Office (SEA-DO)
2/2/2016
86LPLLENSES, SOFT CONTACT, DAILY WEAR
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
333LACKS FIRM
508NO 510(K)
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is Uniqso Holdings Sdn Bhd's FDA import refusal history?

Uniqso Holdings Sdn Bhd (FEI: 3011990635) has 8 FDA import refusal record(s) in our database, spanning from 2/2/2016 to 8/24/2020.

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. Uniqso Holdings Sdn Bhd's FEI number is 3011990635.

What types of violations has Uniqso Holdings Sdn Bhd received?

Uniqso Holdings Sdn Bhd has been cited for 7 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 Uniqso Holdings Sdn Bhd come from?

All FDA import refusal data for Uniqso Holdings Sdn Bhd 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.