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F.T.PHARMA

⚠️ Moderate Risk

FEI: 3009987530 • Ho Chi Minh, VN-65 • VIETNAM

FEI

FEI Number

3009987530

📍

Location

Ho Chi Minh, VN-65

🇻🇳

Country

VIETNAM
🏢

Address

930c2 C Street. Cat Lai Industrial Park, Section 2. Thanh My Loi Ward, District 2, Ho Chi Minh, VN-65, Vietnam

Moderate Risk

FDA Import Risk Assessment

45.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
9/23/2013
Latest Refusal
9/23/2013
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

753×

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).

Refusal History

DateProductViolationsDivision
9/23/2013
54FYH99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
75UNAPPROVED
Cincinnati District Office (CIN-DO)
9/23/2013
54FYH99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
75UNAPPROVED
Cincinnati District Office (CIN-DO)
9/23/2013
54FYH99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
75UNAPPROVED
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is F.T.PHARMA's FDA import refusal history?

F.T.PHARMA (FEI: 3009987530) has 3 FDA import refusal record(s) in our database, spanning from 9/23/2013 to 9/23/2013.

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. F.T.PHARMA's FEI number is 3009987530.

What types of violations has F.T.PHARMA received?

F.T.PHARMA has been cited for 1 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 F.T.PHARMA come from?

All FDA import refusal data for F.T.PHARMA 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.