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Asian Secrets Sdn Bhd

⚠️ Moderate Risk

FEI: 3010814679 • Kuala Lumpur, Wp Kuala Lumpur • MALAYSIA

FEI

FEI Number

3010814679

📍

Location

Kuala Lumpur, Wp Kuala Lumpur

🇲🇾

Country

MALAYSIA
🏢

Address

No. 5 Jalan 4, C-11-4, 5&6, Wisma Goshen, Bangsar Tade Center, Plaza Pantai, Kuala Lumpur, Wp Kuala Lumpur, Malaysia

Moderate Risk

FDA Import Risk Assessment

31.1
LowModerateHighCritical

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

Statistics

4
Total Refusals
10
Unique Violations
9/15/2017
Latest Refusal
2/2/2016
Earliest Refusal

Score Breakdown

Violation Severity
52.1×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
24.7×10%
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

4824×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

4883×

HEALTH C

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling bears an unauthorized nutrient content/health claim.

753×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

2562×

INCONSPICU

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

4732×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

3281×

USUAL NAME

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.

2181×

LIST INGRE

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

22801×

DIRSEXMPT

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a drug within the meaning of Section 201(g) and it lacks adequate directions for use.

3211×

LACKS N/C

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.

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.

Refusal History

DateProductViolationsDivision
9/15/2017
21AYY20CITRUS AND OTHER FRUITS, MIXED
482NUTRIT LBL
75UNAPPROVED
Division of Southeast Imports (DSEI)
4/8/2016
21SCT99SUBTROPICAL AND TROPICAL FRUIT, N.E.C.
2280DIRSEXMPT
256INCONSPICU
473LABELING
482NUTRIT LBL
488HEALTH C
75UNAPPROVED
Seattle District Office (SEA-DO)
4/8/2016
21SHT99SUBTROPICAL AND TROPICAL FRUIT, N.E.C.
16DIRECTIONS
256INCONSPICU
473LABELING
482NUTRIT LBL
488HEALTH C
75UNAPPROVED
Seattle District Office (SEA-DO)
2/2/2016
21BHH09OTHER FRUITS, MIXED, DRIED OR PASTE
218LIST INGRE
321LACKS N/C
328USUAL NAME
482NUTRIT LBL
488HEALTH C
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Asian Secrets Sdn Bhd's FDA import refusal history?

Asian Secrets Sdn Bhd (FEI: 3010814679) has 4 FDA import refusal record(s) in our database, spanning from 2/2/2016 to 9/15/2017.

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. Asian Secrets Sdn Bhd's FEI number is 3010814679.

What types of violations has Asian Secrets Sdn Bhd received?

Asian Secrets Sdn Bhd has been cited for 10 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 Asian Secrets Sdn Bhd come from?

All FDA import refusal data for Asian Secrets 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.