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Jason Aw

⚠️ Moderate Risk

FEI: 3011573934 • Kuala Lumpur, Wilayah Persekutuan • MALAYSIA

FEI

FEI Number

3011573934

📍

Location

Kuala Lumpur, Wilayah Persekutuan

🇲🇾

Country

MALAYSIA
🏢

Address

63-1,Block E,Platinum Walk Taman Danau, , Kuala Lumpur, Wilayah Persekutuan, Malaysia

Moderate Risk

FDA Import Risk Assessment

48.3
LowModerateHighCritical

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

Statistics

23
Total Refusals
6
Unique Violations
4/15/2020
Latest Refusal
5/21/2019
Earliest Refusal

Score Breakdown

Violation Severity
57.3×40%
Refusal Volume
51.1×30%
Recency
0.0×20%
Frequency
100.0×10%
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

11821×

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).

328019×

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.

50818×

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.

24809×

RXPERSONAL

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

3332×

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.

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
4/15/2020
86LPLLENSES, SOFT CONTACT, DAILY WEAR
118NOT LISTED
3280FRNMFGREG
333LACKS FIRM
508NO 510(K)
Division of Southeast Imports (DSEI)
1/16/2020
86HQDLENS, CONTACT (OTHER MATERIAL) - DAILY
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Northern Border Imports (DNBI)
12/30/2019
86LPLLENSES, SOFT CONTACT, DAILY WEAR
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Northern Border Imports (DNBI)
12/3/2019
86LPLLENSES, SOFT CONTACT, DAILY WEAR
118NOT LISTED
2480RXPERSONAL
3280FRNMFGREG
508NO 510(K)
Division of Northern Border Imports (DNBI)
12/3/2019
86MVNLENS, CONTACT (DISPOSABLE)
118NOT LISTED
2480RXPERSONAL
3280FRNMFGREG
508NO 510(K)
Division of Northern Border Imports (DNBI)
12/2/2019
86LPLLENSES, SOFT CONTACT, DAILY WEAR
118NOT LISTED
2480RXPERSONAL
3280FRNMFGREG
508NO 510(K)
Division of Northern Border Imports (DNBI)
11/26/2019
86HQGLENS, SPECTACLE, NON-CUSTOM (PRESCRIPTION)
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
11/20/2019
86LPLLENSES, SOFT CONTACT, DAILY WEAR
118NOT LISTED
2480RXPERSONAL
3280FRNMFGREG
508NO 510(K)
Division of Northern Border Imports (DNBI)
11/18/2019
86LRXCASE, CONTACT LENS
118NOT LISTED
3280FRNMFGREG
Division of Northern Border Imports (DNBI)
11/16/2019
86MVNLENS, CONTACT (DISPOSABLE)
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Northern Border Imports (DNBI)
11/16/2019
86MVNLENS, CONTACT (DISPOSABLE)
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Northern Border Imports (DNBI)
11/16/2019
86MVNLENS, CONTACT (DISPOSABLE)
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Northern Border Imports (DNBI)
11/16/2019
86MVNLENS, CONTACT (DISPOSABLE)
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Northern Border Imports (DNBI)
11/16/2019
86MVNLENS, CONTACT (DISPOSABLE)
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Northern Border Imports (DNBI)
11/13/2019
86LPLLENSES, SOFT CONTACT, DAILY WEAR
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Northern Border Imports (DNBI)
11/13/2019
86LPMLENSES, SOFT CONTACT, EXTENDED WEAR
118NOT LISTED
3280FRNMFGREG
Division of Northern Border Imports (DNBI)
11/13/2019
86LPMLENSES, SOFT CONTACT, EXTENDED WEAR
118NOT LISTED
2480RXPERSONAL
3280FRNMFGREG
508NO 510(K)
Division of Northern Border Imports (DNBI)
11/8/2019
86LRXCASE, CONTACT LENS
118NOT LISTED
Division of Northern Border Imports (DNBI)
10/31/2019
86LPMLENSES, SOFT CONTACT, EXTENDED WEAR
118NOT LISTED
2480RXPERSONAL
3280FRNMFGREG
508NO 510(K)
Division of Northern Border Imports (DNBI)
10/31/2019
86LPLLENSES, SOFT CONTACT, DAILY WEAR
118NOT LISTED
508NO 510(K)
Division of Northern Border Imports (DNBI)
6/11/2019
86LPLLENSES, SOFT CONTACT, DAILY WEAR
2480RXPERSONAL
84RX DEVICE
Division of Southeast Imports (DSEI)
6/11/2019
86LPLLENSES, SOFT CONTACT, DAILY WEAR
2480RXPERSONAL
84RX DEVICE
Division of Southeast Imports (DSEI)
5/21/2019
86LPLLENSES, SOFT CONTACT, DAILY WEAR
118NOT LISTED
2480RXPERSONAL
3280FRNMFGREG
333LACKS FIRM
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Jason Aw's FDA import refusal history?

Jason Aw (FEI: 3011573934) has 23 FDA import refusal record(s) in our database, spanning from 5/21/2019 to 4/15/2020.

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. Jason Aw's FEI number is 3011573934.

What types of violations has Jason Aw received?

Jason Aw 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 Jason Aw come from?

All FDA import refusal data for Jason Aw 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.