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AmMed Supply Co.,Ltd.

⚠️ Moderate Risk

FEI: 3014788869 • Watthana, Krung Thep Maha Nakhon [Bangko • THAILAND

FEI

FEI Number

3014788869

📍

Location

Watthana, Krung Thep Maha Nakhon [Bangko

🇹🇭

Country

THAILAND
🏢

Address

92 Soi Sukhumvit65, , Watthana, Krung Thep Maha Nakhon [Bangko, Thailand

Moderate Risk

FDA Import Risk Assessment

33.2
LowModerateHighCritical

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

Statistics

4
Total Refusals
7
Unique Violations
4/21/2021
Latest Refusal
11/9/2016
Earliest Refusal

Score Breakdown

Violation Severity
61.4×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
9.0×10%
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

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).

2511×

POISONOUS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a poisonous or deleterious substance which may render the article injurious to health. Contains:

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.

32801×

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.

4821×

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.

621×

NEEDS FCE

It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).

831×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

Refusal History

DateProductViolationsDivision
4/21/2021
60LAO99ANALGESIC, N.E.C.
118NOT LISTED
3280FRNMFGREG
Division of Northeast Imports (DNEI)
4/20/2020
23AGH14BETEL NUT, IN SHELL
251POISONOUS
Division of Northeast Imports (DNEI)
11/9/2016
16ACP99FISH, N.E.C.
321LACKS N/C
482NUTRIT LBL
Division of Northeast Imports (DNEI)
11/9/2016
37BEE99MULTIPLE FOOD SPECIALITIES, SIDE DISHES AND DESSERTS, N.E.C.
62NEEDS FCE
83NO PROCESS
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is AmMed Supply Co.,Ltd.'s FDA import refusal history?

AmMed Supply Co.,Ltd. (FEI: 3014788869) has 4 FDA import refusal record(s) in our database, spanning from 11/9/2016 to 4/21/2021.

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. AmMed Supply Co.,Ltd.'s FEI number is 3014788869.

What types of violations has AmMed Supply Co.,Ltd. received?

AmMed Supply Co.,Ltd. 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 AmMed Supply Co.,Ltd. come from?

All FDA import refusal data for AmMed Supply Co.,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.