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Botica Kibrahae

⚠️ Moderate Risk

FEI: 3002661864 • Oranjestad • ARUBA

FEI

FEI Number

3002661864

📍

Location

Oranjestad

🇦🇼

Country

ARUBA
🏢

Address

Arendstraat 30, , Oranjestad, , Aruba

Moderate Risk

FDA Import Risk Assessment

35.3
LowModerateHighCritical

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

Statistics

5
Total Refusals
1
Unique Violations
12/3/2003
Latest Refusal
1/6/2002
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
28.8×30%
Recency
0.0×20%
Frequency
26.2×10%
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

1795×

AGR RX

The article appears to be a prescription drug manufactured in the U.S. and offered for import by other than the manufacturer and reimportation does not appear to have been authorized by the Secretary for use in a medical emergency.

Refusal History

DateProductViolationsDivision
12/3/2003
61XCP99ANTI-HISTAMINIC N.E.C.
179AGR RX
New Orleans District Office (NOL-DO)
1/6/2002
66VCP99MISCELLANEOUS PATENT MEDICINES, ETC.
179AGR RX
New Orleans District Office (NOL-DO)
1/6/2002
66VCP99MISCELLANEOUS PATENT MEDICINES, ETC.
179AGR RX
New Orleans District Office (NOL-DO)
1/6/2002
66VCP99MISCELLANEOUS PATENT MEDICINES, ETC.
179AGR RX
New Orleans District Office (NOL-DO)
1/6/2002
66VCP99MISCELLANEOUS PATENT MEDICINES, ETC.
179AGR RX
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Botica Kibrahae's FDA import refusal history?

Botica Kibrahae (FEI: 3002661864) has 5 FDA import refusal record(s) in our database, spanning from 1/6/2002 to 12/3/2003.

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. Botica Kibrahae's FEI number is 3002661864.

What types of violations has Botica Kibrahae received?

Botica Kibrahae 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 Botica Kibrahae come from?

All FDA import refusal data for Botica Kibrahae 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.