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T.T.I CO., LTD

⚠️ Moderate Risk

FEI: 3013195561 • Ho Chi Minh • VIETNAM

FEI

FEI Number

3013195561

📍

Location

Ho Chi Minh

🇻🇳

Country

VIETNAM
🏢

Address

Rong, P. an Lac A, Q. Binh Tan, NO. 31E, Str No 8,An Lac, Ho Chi Minh, , Vietnam

Moderate Risk

FDA Import Risk Assessment

34.4
LowModerateHighCritical

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

Statistics

4
Total Refusals
5
Unique Violations
9/11/2017
Latest Refusal
6/27/2017
Earliest Refusal

Score Breakdown

Violation Severity
56.7×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
40.0×10%
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

20002×

IMPTRHACCP

The food appears to have been prepared, packed or held under insanitary conditions, or may have become injurious to health, due to the failure of the importer to provide verification of compliance pursuant to 21 CFR 123.12(d).

25801×

MFRHACCP

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the Act in that it appears to have been prepared, packed or held under insanitary conditions whereby it may have been rendered injurious to health in that it appears to have been processed in violation of 21 CFR 123.6(a) and 123.8(a).

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.

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
9/11/2017
16MVY07CUTTLEFISH, OTHER AQUATIC SPECIES
2580MFRHACCP
Division of Southeast Imports (DSEI)
9/11/2017
24HYH08PEPPER, HOT, DRIED OR PASTE
320LACKS FIRM
321LACKS N/C
328USUAL NAME
Division of Southeast Imports (DSEI)
6/27/2017
16AYH99FISH, N.E.C.
2000IMPTRHACCP
Division of Southeast Imports (DSEI)
6/27/2017
16RYH03SHRIMP, IMITATION
2000IMPTRHACCP
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is T.T.I CO., LTD's FDA import refusal history?

T.T.I CO., LTD (FEI: 3013195561) has 4 FDA import refusal record(s) in our database, spanning from 6/27/2017 to 9/11/2017.

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. T.T.I CO., LTD's FEI number is 3013195561.

What types of violations has T.T.I CO., LTD received?

T.T.I CO., LTD has been cited for 5 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 T.T.I CO., LTD come from?

All FDA import refusal data for T.T.I 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.