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Synthite Industries Limited

⚠️ High Risk

FEI: 3004269765 • Kochi, Kerala • INDIA

FEI

FEI Number

3004269765

📍

Location

Kochi, Kerala

🇮🇳

Country

INDIA
🏢

Address

Synthite Valley, Kadayiruppu, Kolenchery, Ernakulam District, Kerela, Kochi, Kerala, India

High Risk

FDA Import Risk Assessment

62.4
LowModerateHighCritical

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

Statistics

13
Total Refusals
8
Unique Violations
5/2/2025
Latest Refusal
4/6/2005
Earliest Refusal

Score Breakdown

Violation Severity
86.4×40%
Refusal Volume
42.5×30%
Recency
72.0×20%
Frequency
6.5×10%
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

2386×

UNSAFE ADD

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.

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).

2491×

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.

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)).

29201×

PESTICIDES

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be adulterated because it contains a pesticide chemical, which is in violation of section 402(a)(2)(B). Contains:

37211×

PESTICIDE2

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be adulterated because it contains a pesticide chemical, which is in violation of section 402(a)(2)(B). Contains:

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.

21201×

UNSFDIETSP

The article appears to be a dietary supplement or ingredient for which there is inadequate information to provide reasonable assurance that such ingredient does not present a significant or unreasonable risk of illness or injury.

Refusal History

DateProductViolationsDivision
5/2/2025
54YBI99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
11UNSAFE COL
Division of Southwest Imports (DSWI)
5/2/2025
54YBI99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
11UNSAFE COL
Division of Southwest Imports (DSWI)
8/10/2022
45LY99FLAVORING AGENTS AND ADJUVANTS (FOOD ADDITIVES FOR HUMAN USE)
249FILTHY
Division of Northeast Imports (DNEI)
6/30/2020
54JYY12KRATOM (HERBAL AND BOTANICAL TEAS II, CONTINUED)
2120UNSFDIETSP
Division of Southeast Imports (DSEI)
5/10/2012
28BGH08CAPSICUMS (CAYENNE CHILI, HOT PEPPERS), GROUND, CRACKED (SPICE)
3721PESTICIDE2
Chicago District Office (CHI-DO)
12/19/2011
24HGH08PEPPER, HOT, DRIED OR PASTE
238UNSAFE ADD
New York District Office (NYK-DO)
12/19/2011
24HFH08PEPPER, HOT, DRIED OR PASTE
238UNSAFE ADD
New York District Office (NYK-DO)
2/19/2011
24HFH08PEPPER, HOT, DRIED OR PASTE
238UNSAFE ADD
Chicago District Office (CHI-DO)
9/24/2008
28BEY54PEPPER, BLACK, GROUND, CRACKED (SPICE)
9SALMONELLA
New Orleans District Office (NOL-DO)
3/1/2006
28AAH08CAPSICUMS (CAYENNE CHILI, HOT PEPPERS), WHOLE (SPICE)
2920PESTICIDES
Southwest Import District Office (SWI-DO)
8/23/2005
28AAH08CAPSICUMS (CAYENNE CHILI, HOT PEPPERS), WHOLE (SPICE)
238UNSAFE ADD
Southwest Import District Office (SWI-DO)
6/14/2005
28BAB08CAPSICUMS (CAYENNE CHILI, HOT PEPPERS), GROUND, CRACKED (SPICE)
238UNSAFE ADD
Southwest Import District Office (SWI-DO)
4/6/2005
28AAB08CAPSICUMS (CAYENNE CHILI, HOT PEPPERS), WHOLE (SPICE)
238UNSAFE ADD
256INCONSPICU
Division of Southwest Imports (DSWI)

Frequently Asked Questions

What is Synthite Industries Limited's FDA import refusal history?

Synthite Industries Limited (FEI: 3004269765) has 13 FDA import refusal record(s) in our database, spanning from 4/6/2005 to 5/2/2025.

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. Synthite Industries Limited's FEI number is 3004269765.

What types of violations has Synthite Industries Limited received?

Synthite Industries Limited has been cited for 8 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 Synthite Industries Limited come from?

All FDA import refusal data for Synthite Industries 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.