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CHAIPHATANA LIMITED

⚠️ Moderate Risk

FEI: 3013306040 • Khokod, Pathum Thani • THAILAND

FEI

FEI Number

3013306040

📍

Location

Khokod, Pathum Thani

🇹🇭

Country

THAILAND
🏢

Address

1 60-62 Moo 1, Chomchonchawfar, Lumlookka, Khokod, Pathum Thani, Thailand

Moderate Risk

FDA Import Risk Assessment

43.6
LowModerateHighCritical

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

Statistics

8
Total Refusals
6
Unique Violations
7/8/2019
Latest Refusal
11/9/2011
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
35.3×30%
Recency
0.0×20%
Frequency
10.4×10%
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

32403×

NOCONTCODE

The low acid or acidified food appears to have been prepared, packed, or held under insanitary conditions, or it may be injurious to health, due to failure to mark with a permanent container code pursuant to 21 CFR 113.60(c) or 114.80(b).

112×

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).

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.

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.

91×

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.

Refusal History

DateProductViolationsDivision
7/8/2019
37JCT03CHILI SAUCE
11UNSAFE COL
Division of Northern Border Imports (DNBI)
8/31/2017
28AGT04BASIL (SWEET BASIL), WHOLE (SPICE)
9SALMONELLA
Division of West Coast Imports (DWCI)
1/9/2015
28JCT99MIXED SPICES AND SEASONING WITH SALT, N.E.C.
3240NOCONTCODE
Minneapolis District Office (MIN-DO)
1/9/2015
37JCI03CHILI SAUCE
3240NOCONTCODE
Minneapolis District Office (MIN-DO)
1/9/2015
24VEE03BAMBOO SHOOTS, WITH SAUCE
3240NOCONTCODE
Minneapolis District Office (MIN-DO)
7/1/2014
24TGE03BAMBOO SHOOTS (LEAF & STEM VEGETABLE)
62NEEDS FCE
Los Angeles District Office (LOS-DO)
5/15/2014
02HGH01TAPIOCA STARCH PRODUCT
11UNSAFE COL
218LIST INGRE
Seattle District Office (SEA-DO)
11/9/2011
24TCE03BAMBOO SHOOTS (LEAF & STEM VEGETABLE)
83NO PROCESS
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is CHAIPHATANA LIMITED's FDA import refusal history?

CHAIPHATANA LIMITED (FEI: 3013306040) has 8 FDA import refusal record(s) in our database, spanning from 11/9/2011 to 7/8/2019.

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. CHAIPHATANA LIMITED's FEI number is 3013306040.

What types of violations has CHAIPHATANA LIMITED received?

CHAIPHATANA LIMITED has been cited for 6 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 CHAIPHATANA LIMITED come from?

All FDA import refusal data for CHAIPHATANA LIMITED 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.