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Camilo Vasco Ceballos

✅ Low Risk

FEI: 3010359200 • Sabaneta, Antioquia • COLOMBIA

FEI

FEI Number

3010359200

📍

Location

Sabaneta, Antioquia

🇨🇴

Country

COLOMBIA
🏢

Address

Carrera 44b 64bs 35, , Sabaneta, Antioquia, Colombia

Low Risk

FDA Import Risk Assessment

23.3
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

1
Total Refusals
4
Unique Violations
10/16/2013
Latest Refusal
10/16/2013
Earliest Refusal

Score Breakdown

Violation Severity
47.5×40%
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).

2311×

LENS CERT

The lenses are declared by accompanying certificate to meet the requirements for impact-resistant lenses in 21 CFR 801.410 but does not appear to be impact-resistant.

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

37411×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(o) in that it is being imported or offered for import into the United States, and the importer, owner, or consignee of such article did not, at the time of offering the article for import, submit to the Secretary a statement that identifies the registration under section 510(i) of the Act of each establishment that with respect to such article is required under such section to register with the Secretary.

Refusal History

DateProductViolationsDivision
10/16/2013
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
231LENS CERT
3280FRNMFGREG
3741FRNMFGREG
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Camilo Vasco Ceballos's FDA import refusal history?

Camilo Vasco Ceballos (FEI: 3010359200) has 1 FDA import refusal record(s) in our database, spanning from 10/16/2013 to 10/16/2013.

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. Camilo Vasco Ceballos's FEI number is 3010359200.

What types of violations has Camilo Vasco Ceballos received?

Camilo Vasco Ceballos has been cited for 4 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 Camilo Vasco Ceballos come from?

All FDA import refusal data for Camilo Vasco Ceballos 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.