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UD Herba Asli

⚠️ Moderate Risk

FEI: 3009348564 • Medan, Sumatera utara • INDONESIA

FEI

FEI Number

3009348564

📍

Location

Medan, Sumatera utara

🇮🇩

Country

INDONESIA
🏢

Address

Jln. Jumhana 11c, , Medan, Sumatera utara, Indonesia

Moderate Risk

FDA Import Risk Assessment

39.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
7/6/2012
Latest Refusal
7/6/2012
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

751×

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
7/6/2012
54FDR99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
75UNAPPROVED
Seattle District Office (SEA-DO)
7/6/2012
66BCS99STIMULANT N.E.C.
16DIRECTIONS
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is UD Herba Asli's FDA import refusal history?

UD Herba Asli (FEI: 3009348564) has 2 FDA import refusal record(s) in our database, spanning from 7/6/2012 to 7/6/2012.

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. UD Herba Asli's FEI number is 3009348564.

What types of violations has UD Herba Asli received?

UD Herba Asli 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 UD Herba Asli come from?

All FDA import refusal data for UD Herba Asli 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.