SAMSUNG SDS-HCM 2300680991001
⚠️ Moderate Risk
FEI: 3031869540 • Buu Cuc Trung Tam Thanh Pho Ho Chi Minh, Ho Chi Minh • VIETNAM
FEI Number
3031869540
Location
Buu Cuc Trung Tam Thanh Pho Ho Chi Minh, Ho Chi Minh
Country
VIETNAMAddress
6th Floor, Scs Building, , Buu Cuc Trung Tam Thanh Pho Ho Chi Minh, Ho Chi Minh, Vietnam
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
NO ENGLISH
Required label or labeling appears to not be in English in violation of 21 C.F.R. 201.15(c)(1).
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
Frequently Asked Questions
What is SAMSUNG SDS-HCM 2300680991001's FDA import refusal history?
SAMSUNG SDS-HCM 2300680991001 (FEI: 3031869540) has 1 FDA import refusal record(s) in our database, spanning from 9/27/2024 to 9/27/2024.
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. SAMSUNG SDS-HCM 2300680991001's FEI number is 3031869540.
What types of violations has SAMSUNG SDS-HCM 2300680991001 received?
SAMSUNG SDS-HCM 2300680991001 has been cited for 2 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 SAMSUNG SDS-HCM 2300680991001 come from?
All FDA import refusal data for SAMSUNG SDS-HCM 2300680991001 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.