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Leonelia Izquierdo

⚠️ Moderate Risk

FEI: 3009107637 • Calicali • COLOMBIA

FEI

FEI Number

3009107637

📍

Location

Calicali

🇨🇴

Country

COLOMBIA
🏢

Address

Calle 17 No 9- 30villa Gorgona, , Calicali, , Colombia

Moderate Risk

FDA Import Risk Assessment

32.9
LowModerateHighCritical

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

Statistics

2
Total Refusals
5
Unique Violations
10/6/2011
Latest Refusal
10/6/2011
Earliest Refusal

Score Breakdown

Violation Severity
64.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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).

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).

3411×

REGISTERED

It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).

5081×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

751×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

Refusal History

DateProductViolationsDivision
10/6/2011
74DQFACTUATOR, SYRINGE, INJECTOR TYPE
118NOT LISTED
341REGISTERED
508NO 510(K)
Cincinnati District Office (CIN-DO)
10/6/2011
65JCY01ALGESTONE ACETOPHENIDE (PROGESTIN)
27DRUG GMPS
75UNAPPROVED
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Leonelia Izquierdo's FDA import refusal history?

Leonelia Izquierdo (FEI: 3009107637) has 2 FDA import refusal record(s) in our database, spanning from 10/6/2011 to 10/6/2011.

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. Leonelia Izquierdo's FEI number is 3009107637.

What types of violations has Leonelia Izquierdo received?

Leonelia Izquierdo has been cited for 5 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 Leonelia Izquierdo come from?

All FDA import refusal data for Leonelia Izquierdo 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.