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Jin Jin Marketing

⚠️ Moderate Risk

FEI: 3002363237 • Bangkok, TH-10 • THAILAND

FEI

FEI Number

3002363237

📍

Location

Bangkok, TH-10

🇹🇭

Country

THAILAND
🏢

Address

3333/16-17 Suprasert Road, Bangklo, Bangkorlaem, , Bangkok, TH-10, Thailand

Moderate Risk

FDA Import Risk Assessment

46.3
LowModerateHighCritical

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

Statistics

23
Total Refusals
17
Unique Violations
2/1/2018
Latest Refusal
7/21/2003
Earliest Refusal

Score Breakdown

Violation Severity
73.3×40%
Refusal Volume
51.1×30%
Recency
0.0×20%
Frequency
15.8×10%
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

115×

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).

834×

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.

2494×

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.

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).

624×

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).

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.

4832×

DRUG NAME

The article appears to be a drug and fails to bear the proprietary or established name and/or name and quantity of each active ingredient.

92×

SALMONELLA

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

1182×

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).

162×

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.

2512×

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:

3082×

MFR INSAN

The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.

4722×

NO ENGLISH

Required label or labeling appears to not be in English in violation of 21 C.F.R. 201.15(c)(1).

3241×

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)).

3201×

LACKS FIRM

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)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.

2741×

COLOR LBLG

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

2561×

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)).

Refusal History

DateProductViolationsDivision
2/1/2018
28AGH13CINNAMON, CASSIA, WHOLE (SPICE)
249FILTHY
Division of West Coast Imports (DWCI)
10/26/2012
53GH02FACE POWDERS (MAKEUP PREPARATIONS, NOT FOR EYES)
251POISONOUS
Los Angeles District Office (LOS-DO)
10/26/2012
53GH02FACE POWDERS (MAKEUP PREPARATIONS, NOT FOR EYES)
251POISONOUS
Los Angeles District Office (LOS-DO)
10/26/2012
53ED06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING)
75UNAPPROVED
Los Angeles District Office (LOS-DO)
10/26/2012
53ED06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING)
75UNAPPROVED
Los Angeles District Office (LOS-DO)
10/26/2012
53ED06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING)
75UNAPPROVED
Los Angeles District Office (LOS-DO)
10/26/2012
53ED06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING)
75UNAPPROVED
Los Angeles District Office (LOS-DO)
2/27/2012
24HGH08PEPPER, HOT, DRIED OR PASTE
9SALMONELLA
San Francisco District Office (SAN-DO)
11/20/2009
28AGH08CAPSICUMS (CAYENNE CHILI, HOT PEPPERS), WHOLE (SPICE)
249FILTHY
308MFR INSAN
Los Angeles District Office (LOS-DO)
8/25/2009
28BHT08CAPSICUMS (CAYENNE CHILI, HOT PEPPERS), GROUND, CRACKED (SPICE)
249FILTHY
308MFR INSAN
Los Angeles District Office (LOS-DO)
11/15/2008
24UGH99LEAF & STEM VEGETABLES, DRIED OR PASTE, N.E.C.
249FILTHY
Los Angeles District Office (LOS-DO)
3/3/2007
64AAR99DISINFECTANT N.E.C.
118NOT LISTED
16DIRECTIONS
472NO ENGLISH
483DRUG NAME
San Francisco District Office (SAN-DO)
3/3/2007
64AAR99DISINFECTANT N.E.C.
118NOT LISTED
16DIRECTIONS
472NO ENGLISH
483DRUG NAME
San Francisco District Office (SAN-DO)
12/2/2005
02HGT01TAPIOCA STARCH PRODUCT
11UNSAFE COL
Los Angeles District Office (LOS-DO)
10/21/2005
28BCT54PEPPER, BLACK, GROUND, CRACKED (SPICE)
9SALMONELLA
Los Angeles District Office (LOS-DO)
8/1/2003
29AGT07SOFT DRINK, SUBTROPICAL OR TROPICAL FRUIT FLAVORED, NONCARBONATED
62NEEDS FCE
83NO PROCESS
San Francisco District Office (SAN-DO)
8/1/2003
29AGT07SOFT DRINK, SUBTROPICAL OR TROPICAL FRUIT FLAVORED, NONCARBONATED
62NEEDS FCE
83NO PROCESS
San Francisco District Office (SAN-DO)
8/1/2003
29AGT07SOFT DRINK, SUBTROPICAL OR TROPICAL FRUIT FLAVORED, NONCARBONATED
62NEEDS FCE
83NO PROCESS
San Francisco District Office (SAN-DO)
8/1/2003
29AGT07SOFT DRINK, SUBTROPICAL OR TROPICAL FRUIT FLAVORED, NONCARBONATED
62NEEDS FCE
83NO PROCESS
San Francisco District Office (SAN-DO)
8/1/2003
35AGT01GELATIN, FLAVORED
11UNSAFE COL
324NO ENGLISH
San Francisco District Office (SAN-DO)
8/1/2003
35AGT01GELATIN, FLAVORED
11UNSAFE COL
218LIST INGRE
San Francisco District Office (SAN-DO)
8/1/2003
35AGT01GELATIN, FLAVORED
11UNSAFE COL
218LIST INGRE
San Francisco District Office (SAN-DO)
7/21/2003
33EGT06FLAVORED CANDY, HARD (LIVE SAVERS, ETC.), WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
11UNSAFE COL
218LIST INGRE
256INCONSPICU
274COLOR LBLG
320LACKS FIRM
San Francisco District Office (SAN-DO)

Frequently Asked Questions

What is Jin Jin Marketing's FDA import refusal history?

Jin Jin Marketing (FEI: 3002363237) has 23 FDA import refusal record(s) in our database, spanning from 7/21/2003 to 2/1/2018.

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. Jin Jin Marketing's FEI number is 3002363237.

What types of violations has Jin Jin Marketing received?

Jin Jin Marketing has been cited for 17 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 Jin Jin Marketing come from?

All FDA import refusal data for Jin Jin Marketing 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.