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Anggia

⚠️ Moderate Risk

FEI: 3011853014 • Bandungbandung • INDONESIA

FEI

FEI Number

3011853014

📍

Location

Bandungbandung

🇮🇩

Country

INDONESIA
🏢

Address

Jl Setia Budi No 52 Karang Tengah, , Bandungbandung, , Indonesia

Moderate Risk

FDA Import Risk Assessment

36.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
2/29/2016
Latest Refusal
2/29/2016
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

22001×

DIET INGRE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be for use as an ingredient in a dietary supplement and appears to be or may be otherwise unfit for food.

Refusal History

DateProductViolationsDivision
2/29/2016
54EYY95BANABA (HERBAL & BOTANICAL TEAS)
2200DIET INGRE
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Anggia's FDA import refusal history?

Anggia (FEI: 3011853014) has 1 FDA import refusal record(s) in our database, spanning from 2/29/2016 to 2/29/2016.

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. Anggia's FEI number is 3011853014.

What types of violations has Anggia received?

Anggia 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 Anggia come from?

All FDA import refusal data for Anggia 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.