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Shwe Hinthar Yeik Mon Co., Ltd.

⚠️ High Risk

FEI: 3012044720 • Bago, Bago • MYANMAR

FEI

FEI Number

3012044720

📍

Location

Bago, Bago

🇲🇲

Country

MYANMAR
🏢

Address

No.38, Nyaung Inn Street, Oakthar Myothit, Local Industrial Zone, Bago, Bago, Myanmar

High Risk

FDA Import Risk Assessment

60.6
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

17
Total Refusals
16
Unique Violations
1/28/2025
Latest Refusal
7/7/2015
Earliest Refusal

Score Breakdown

Violation Severity
71.8×40%
Refusal Volume
46.5×30%
Recency
81.0×20%
Frequency
17.8×10%
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

2515×

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:

2183×

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.

2493×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

113×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

4822×

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.

642×

YELLOW #5

The food appears to bear or contain the color additive FD & C Yellow No. 5, which is not declared on the label per 21 CFR 74.705(a)(c) under section 721.

34001×

PB-FOOD

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

38981×

INADPRCCTL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health due to inadequate process controls.

4731×

LABELING

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

481×

NEEDS ACID

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health due to inadequate acidification.

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.

23601×

HISTAMINE

The article appears to bear or contain histamine, a poisonous and deleterious substance in such quantity as ordinarily renders it injurious to health.

2601×

FALSE

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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.

2741×

COLOR LBLG

The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.

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.

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.

Refusal History

DateProductViolationsDivision
1/28/2025
24FEI99FRUITS USED AS VEGETABLES, N.E.C.
3898INADPRCCTL
48NEEDS ACID
Division of Northeast Imports (DNEI)
5/6/2020
31KFT40TEA, INSTANT MIX (WITH LEMON, SUGAR, ETC.)
260FALSE
Division of Southeast Imports (DSEI)
5/6/2020
31KGT40TEA, INSTANT MIX (WITH LEMON, SUGAR, ETC.)
218LIST INGRE
Division of Southeast Imports (DSEI)
1/15/2020
21HGT14PLUM, DRIED OR PASTE
3400PB-FOOD
Division of Southeast Imports (DSEI)
12/12/2018
24FCY99FRUITS USED AS VEGETABLES, N.E.C.
249FILTHY
Division of Northern Border Imports (DNBI)
3/20/2018
21JGT14PLUM, JAM, JELLY, PRESERVES, MARMALADE, BUTTER OR CANDIED
218LIST INGRE
482NUTRIT LBL
64YELLOW #5
Division of Northern Border Imports (DNBI)
3/20/2018
21KGT14PLUM, JUICE, PIT FRUIT JUICES OR CONCENTRATES
11UNSAFE COL
482NUTRIT LBL
64YELLOW #5
Division of Northern Border Imports (DNBI)
3/20/2018
21JGT14PLUM, JAM, JELLY, PRESERVES, MARMALADE, BUTTER OR CANDIED
11UNSAFE COL
274COLOR LBLG
Division of Northern Border Imports (DNBI)
3/20/2018
21JGT14PLUM, JAM, JELLY, PRESERVES, MARMALADE, BUTTER OR CANDIED
11UNSAFE COL
218LIST INGRE
328USUAL NAME
Division of Northern Border Imports (DNBI)
12/9/2015
16AGT99FISH, N.E.C.
2360HISTAMINE
249FILTHY
Chicago District Office (CHI-DO)
12/9/2015
16AGT99FISH, N.E.C.
249FILTHY
473LABELING
Chicago District Office (CHI-DO)
8/24/2015
24TGT99LEAF & STEM VEGETABLES, N.E.C.
321LACKS N/C
83NO PROCESS
Chicago District Office (CHI-DO)
8/24/2015
23OVY14BETEL NUT, NUT FLOUR/MEAL
251POISONOUS
Chicago District Office (CHI-DO)
8/24/2015
23OVY14BETEL NUT, NUT FLOUR/MEAL
251POISONOUS
Chicago District Office (CHI-DO)
8/24/2015
23OVY14BETEL NUT, NUT FLOUR/MEAL
251POISONOUS
Chicago District Office (CHI-DO)
7/7/2015
23OVY14BETEL NUT, NUT FLOUR/MEAL
251POISONOUS
Chicago District Office (CHI-DO)
7/7/2015
23OVY14BETEL NUT, NUT FLOUR/MEAL
251POISONOUS
Chicago District Office (CHI-DO)

Frequently Asked Questions

What is Shwe Hinthar Yeik Mon Co., Ltd.'s FDA import refusal history?

Shwe Hinthar Yeik Mon Co., Ltd. (FEI: 3012044720) has 17 FDA import refusal record(s) in our database, spanning from 7/7/2015 to 1/28/2025.

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. Shwe Hinthar Yeik Mon Co., Ltd.'s FEI number is 3012044720.

What types of violations has Shwe Hinthar Yeik Mon Co., Ltd. received?

Shwe Hinthar Yeik Mon Co., Ltd. has been cited for 16 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 Shwe Hinthar Yeik Mon Co., Ltd. come from?

All FDA import refusal data for Shwe Hinthar Yeik Mon 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.