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SHWE Hintar Co.

⚠️ High Risk

FEI: 3008986440 • Plaeng Yao, Chachoengsao • THAILAND

FEI

FEI Number

3008986440

📍

Location

Plaeng Yao, Chachoengsao

🇹🇭

Country

THAILAND
🏢

Address

Estate, Thanon Gate Way City Soi 7, Plaeng Yao, Chachoengsao, Thailand

High Risk

FDA Import Risk Assessment

51.9
LowModerateHighCritical

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

Statistics

22
Total Refusals
13
Unique Violations
2/17/2015
Latest Refusal
4/13/2012
Earliest Refusal

Score Breakdown

Violation Severity
72.6×40%
Refusal Volume
50.4×30%
Recency
0.0×20%
Frequency
77.2×10%
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

24912×

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.

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.

163×

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.

1183×

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).

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).

832×

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.

3242×

NO ENGLISH

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)).

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.

4731×

LABELING

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

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.

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).

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:

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.

Refusal History

DateProductViolationsDivision
2/17/2015
23OVY14BETEL NUT, NUT FLOUR/MEAL
249FILTHY
251POISONOUS
Chicago District Office (CHI-DO)
9/8/2014
24AGE13SOYBEANS (SEE INDUSTRY 37 FOR 'BEAN CURD')
83NO PROCESS
Chicago District Office (CHI-DO)
6/27/2014
66VCY99MISCELLANEOUS PATENT MEDICINES, ETC.
16DIRECTIONS
473LABELING
75UNAPPROVED
Chicago District Office (CHI-DO)
8/8/2012
04CGY05NOODLES, WHEAT AND SOY
482NUTRIT LBL
Chicago District Office (CHI-DO)
8/8/2012
16YGH09FISH SAUCE, FISHERY PRODUCTS, N.E.C.
482NUTRIT LBL
Chicago District Office (CHI-DO)
8/8/2012
16AHH01ANCHOVY
324NO ENGLISH
482NUTRIT LBL
Chicago District Office (CHI-DO)
8/8/2012
37JHI03CHILI SAUCE
62NEEDS FCE
83NO PROCESS
Chicago District Office (CHI-DO)
6/29/2012
62MBJ01CAMPHOR (ANTI-PRURITIC)
118NOT LISTED
16DIRECTIONS
75UNAPPROVED
Chicago District Office (CHI-DO)
6/29/2012
62MBJ01CAMPHOR (ANTI-PRURITIC)
118NOT LISTED
16DIRECTIONS
75UNAPPROVED
Chicago District Office (CHI-DO)
5/23/2012
62MBJ01CAMPHOR (ANTI-PRURITIC)
118NOT LISTED
Chicago District Office (CHI-DO)
4/13/2012
16ADH15EEL
249FILTHY
Chicago District Office (CHI-DO)
4/13/2012
16ADH73MACKEREL (ALL EXCEPT SCOMBEROMORUS SP, EG SPANISH OR KING SEE '22')
249FILTHY
Chicago District Office (CHI-DO)
4/13/2012
16ADH99FISH, N.E.C.
249FILTHY
Chicago District Office (CHI-DO)
4/13/2012
16ADH25PIKE, PICKEREL, MUSKELLUNGE
249FILTHY
Chicago District Office (CHI-DO)
4/13/2012
16ADH01ANCHOVY
249FILTHY
Chicago District Office (CHI-DO)
4/13/2012
16ADH64MUD FISH
249FILTHY
Chicago District Office (CHI-DO)
4/13/2012
16ADH64MUD FISH
249FILTHY
Chicago District Office (CHI-DO)
4/13/2012
16ADH24OCEAN PERCH (RED PERCH, PACIFIC PERCH, REDFISH)
249FILTHY
Chicago District Office (CHI-DO)
4/13/2012
16ADH24OCEAN PERCH (RED PERCH, PACIFIC PERCH, REDFISH)
249FILTHY
Chicago District Office (CHI-DO)
4/13/2012
16ADH99FISH, N.E.C.
249FILTHY
Chicago District Office (CHI-DO)
4/13/2012
16ADH99FISH, N.E.C.
249FILTHY
Chicago District Office (CHI-DO)
4/13/2012
04CGY05NOODLES, WHEAT AND SOY
218LIST INGRE
321LACKS N/C
324NO ENGLISH
328USUAL NAME
482NUTRIT LBL
Chicago District Office (CHI-DO)

Frequently Asked Questions

What is SHWE Hintar Co.'s FDA import refusal history?

SHWE Hintar Co. (FEI: 3008986440) has 22 FDA import refusal record(s) in our database, spanning from 4/13/2012 to 2/17/2015.

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 Hintar Co.'s FEI number is 3008986440.

What types of violations has SHWE Hintar Co. received?

SHWE Hintar Co. has been cited for 13 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 Hintar Co. come from?

All FDA import refusal data for SHWE Hintar Co. 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.