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Claudia P Osorio

⚠️ Moderate Risk

FEI: 3009513528 • Santa Fe De Bogotasanta Fe De Bogota • COLOMBIA

FEI

FEI Number

3009513528

📍

Location

Santa Fe De Bogotasanta Fe De Bogota

🇨🇴

Country

COLOMBIA
🏢

Address

Calle 42 # 42-36 Barrio Las Palmas, , Santa Fe De Bogotasanta Fe De Bogota, , Colombia

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
7/26/2012
Latest Refusal
7/26/2012
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

271×

DRUG GMPS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the methods used in and controls used for the manufacture, processing, packing, or holding of drugs and other products do not appear to conform to current good manufacturing practices within the meaning of Section 501(a)(2)(B).

Refusal History

DateProductViolationsDivision
7/26/2012
66VCK99MISCELLANEOUS PATENT MEDICINES, ETC.
27DRUG GMPS
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Claudia P Osorio's FDA import refusal history?

Claudia P Osorio (FEI: 3009513528) has 1 FDA import refusal record(s) in our database, spanning from 7/26/2012 to 7/26/2012.

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. Claudia P Osorio's FEI number is 3009513528.

What types of violations has Claudia P Osorio received?

Claudia P Osorio 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 Claudia P Osorio come from?

All FDA import refusal data for Claudia P Osorio 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.