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Theresia H

⚠️ Moderate Risk

FEI: 3006203515 • Jakarta • INDONESIA

FEI

FEI Number

3006203515

📍

Location

Jakarta

🇮🇩

Country

INDONESIA
🏢

Address

Letjend Supraptokav4, , Jakarta, , Indonesia

Moderate Risk

FDA Import Risk Assessment

33.6
LowModerateHighCritical

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

Statistics

5
Total Refusals
1
Unique Violations
4/27/2007
Latest Refusal
4/27/2007
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
28.8×30%
Recency
0.0×20%
Frequency
50.0×10%
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

1185×

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).

Refusal History

DateProductViolationsDivision
4/27/2007
64HCA99EXPECTORANT N.E.C.
118NOT LISTED
New York District Office (NYK-DO)
4/27/2007
63BCK01ALBUTEROL (BRONCHODILATOR)
118NOT LISTED
New York District Office (NYK-DO)
4/27/2007
64HCK01BROMHEXINE HCL (EXPECTORANT)
118NOT LISTED
New York District Office (NYK-DO)
4/27/2007
64HCA01BROMHEXINE HCL (EXPECTORANT)
118NOT LISTED
New York District Office (NYK-DO)
4/27/2007
65VCA99SEDATIVE N.E.C.
118NOT LISTED
New York District Office (NYK-DO)

Frequently Asked Questions

What is Theresia H's FDA import refusal history?

Theresia H (FEI: 3006203515) has 5 FDA import refusal record(s) in our database, spanning from 4/27/2007 to 4/27/2007.

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. Theresia H's FEI number is 3006203515.

What types of violations has Theresia H received?

Theresia H 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 Theresia H come from?

All FDA import refusal data for Theresia H 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.