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A.M. Herbs (M) Pvt. Ltd.

⚠️ Moderate Risk

FEI: 3004686954 • Kuala Lumpur, MY-14 • MALAYSIA

FEI

FEI Number

3004686954

📍

Location

Kuala Lumpur, MY-14

🇲🇾

Country

MALAYSIA
🏢

Address

2-4 JLN 3/114 Kuchai Business Center, , Kuala Lumpur, MY-14, Malaysia

Moderate Risk

FDA Import Risk Assessment

35.8
LowModerateHighCritical

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

Statistics

5
Total Refusals
4
Unique Violations
5/17/2004
Latest Refusal
5/17/2004
Earliest Refusal

Score Breakdown

Violation Severity
55.4×40%
Refusal Volume
28.8×30%
Recency
0.0×20%
Frequency
50.0×10%
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

4825×

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.

754×

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).

2182×

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.

4732×

LABELING

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

Refusal History

DateProductViolationsDivision
5/17/2004
54YGE99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
482NUTRIT LBL
75UNAPPROVED
Seattle District Office (SEA-DO)
5/17/2004
54FCE99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
482NUTRIT LBL
75UNAPPROVED
Seattle District Office (SEA-DO)
5/17/2004
54YGE99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
482NUTRIT LBL
Seattle District Office (SEA-DO)
5/17/2004
54YCE99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
218LIST INGRE
473LABELING
482NUTRIT LBL
75UNAPPROVED
Seattle District Office (SEA-DO)
5/17/2004
54YBC99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
218LIST INGRE
473LABELING
482NUTRIT LBL
75UNAPPROVED
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is A.M. Herbs (M) Pvt. Ltd.'s FDA import refusal history?

A.M. Herbs (M) Pvt. Ltd. (FEI: 3004686954) has 5 FDA import refusal record(s) in our database, spanning from 5/17/2004 to 5/17/2004.

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. A.M. Herbs (M) Pvt. Ltd.'s FEI number is 3004686954.

What types of violations has A.M. Herbs (M) Pvt. Ltd. received?

A.M. Herbs (M) Pvt. Ltd. has been cited for 4 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 A.M. Herbs (M) Pvt. Ltd. come from?

All FDA import refusal data for A.M. Herbs (M) Pvt. 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.