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PUTRA EDI

⚠️ Moderate Risk

FEI: 3027659145 • Jakarta • INDONESIA

FEI

FEI Number

3027659145

📍

Location

Jakarta

🇮🇩

Country

INDONESIA
🏢

Address

Building, Jl. Mt Haryono Kav 2 -3, Soho Pancoran, Jakarta, , Indonesia

Moderate Risk

FDA Import Risk Assessment

47.8
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
11/19/2023
Latest Refusal
11/19/2023
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
11.2×30%
Recency
57.1×20%
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

39001×

NDIDIETSP

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be a food that is a dietary supplement or that contains a dietary ingredient that is a new dietary ingredient for which there is inadequate information to provide reasonable assurance that such ingredient does not present a significant or unreasonable risk of illness or injury.

Refusal History

DateProductViolationsDivision
11/19/2023
54JBR12KRATOM (HERBAL AND BOTANICAL TEAS II, CONTINUED)
3900NDIDIETSP
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is PUTRA EDI's FDA import refusal history?

PUTRA EDI (FEI: 3027659145) has 1 FDA import refusal record(s) in our database, spanning from 11/19/2023 to 11/19/2023.

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. PUTRA EDI's FEI number is 3027659145.

What types of violations has PUTRA EDI received?

PUTRA EDI 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 PUTRA EDI come from?

All FDA import refusal data for PUTRA EDI 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.