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Pt Citra Raphael Inter

⚠️ Moderate Risk

FEI: 3005396738 • Jakarta, Jabotabek • INDONESIA

FEI

FEI Number

3005396738

📍

Location

Jakarta, Jabotabek

🇮🇩

Country

INDONESIA
🏢

Address

Jln. Danau Sunter Barat, PO, Jakarta, Jabotabek, Indonesia

Moderate Risk

FDA Import Risk Assessment

26.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
8/9/2007
Latest Refusal
8/9/2007
Earliest Refusal

Score Breakdown

Violation Severity
55.0×40%
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

1181×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

2231×

FALSE

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose labeling appears to be false or misleading.

Refusal History

DateProductViolationsDivision
8/9/2007
66VBW99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
223FALSE
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Pt Citra Raphael Inter's FDA import refusal history?

Pt Citra Raphael Inter (FEI: 3005396738) has 1 FDA import refusal record(s) in our database, spanning from 8/9/2007 to 8/9/2007.

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. Pt Citra Raphael Inter's FEI number is 3005396738.

What types of violations has Pt Citra Raphael Inter received?

Pt Citra Raphael Inter 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 Pt Citra Raphael Inter come from?

All FDA import refusal data for Pt Citra Raphael Inter 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.