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Vinhtien Co., Ltd.

⚠️ Moderate Risk

FEI: 3006167812 • Tinh Lam Dong • VIETNAM

FEI

FEI Number

3006167812

📍

Location

Tinh Lam Dong

🇻🇳

Country

VIETNAM
🏢

Address

41 Pham Ngoc Thach Dalat, , Tinh Lam Dong, , Vietnam

Moderate Risk

FDA Import Risk Assessment

41.0
LowModerateHighCritical

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

Statistics

8
Total Refusals
4
Unique Violations
1/15/2014
Latest Refusal
1/15/2014
Earliest Refusal

Score Breakdown

Violation Severity
56.0×40%
Refusal Volume
35.3×30%
Recency
0.0×20%
Frequency
80.0×10%
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

1188×

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).

758×

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).

32807×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

37417×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(o) in that it is being imported or offered for import into the United States, and the importer, owner, or consignee of such article did not, at the time of offering the article for import, submit to the Secretary a statement that identifies the registration under section 510(i) of the Act of each establishment that with respect to such article is required under such section to register with the Secretary.

Refusal History

DateProductViolationsDivision
1/15/2014
62BBY99ANTI-HYPERLIPIDEMIC N.E.C.
118NOT LISTED
3280FRNMFGREG
3741FRNMFGREG
75UNAPPROVED
Los Angeles District Office (LOS-DO)
1/15/2014
65CBY99NUTRIENT/TONIC N.E.C.
118NOT LISTED
3280FRNMFGREG
3741FRNMFGREG
75UNAPPROVED
Los Angeles District Office (LOS-DO)
1/15/2014
60LBY99ANALGESIC, N.E.C.
118NOT LISTED
3280FRNMFGREG
3741FRNMFGREG
75UNAPPROVED
Los Angeles District Office (LOS-DO)
1/15/2014
61PBY99ANTI-DIABETIC N.E.C.
118NOT LISTED
3280FRNMFGREG
3741FRNMFGREG
75UNAPPROVED
Los Angeles District Office (LOS-DO)
1/15/2014
60GAY99ALCOHOL DETERRENT, N.E.C.
118NOT LISTED
3280FRNMFGREG
3741FRNMFGREG
75UNAPPROVED
Los Angeles District Office (LOS-DO)
1/15/2014
62UBY99ANTI-TUSSIVE/COLD N.E.C.
118NOT LISTED
3280FRNMFGREG
3741FRNMFGREG
75UNAPPROVED
Los Angeles District Office (LOS-DO)
1/15/2014
60GAY99ALCOHOL DETERRENT, N.E.C.
118NOT LISTED
3280FRNMFGREG
3741FRNMFGREG
75UNAPPROVED
Los Angeles District Office (LOS-DO)
1/15/2014
61JBY99ANTI-CHOLESTEREMIC, N.E.C.
118NOT LISTED
75UNAPPROVED
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Vinhtien Co., Ltd.'s FDA import refusal history?

Vinhtien Co., Ltd. (FEI: 3006167812) has 8 FDA import refusal record(s) in our database, spanning from 1/15/2014 to 1/15/2014.

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. Vinhtien Co., Ltd.'s FEI number is 3006167812.

What types of violations has Vinhtien Co., Ltd. received?

Vinhtien Co., Ltd. has been cited for 4 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 Vinhtien Co., Ltd. come from?

All FDA import refusal data for Vinhtien 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.