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Laboratorio Kener Sa De Cv

⚠️ Moderate Risk

FEI: 3010029948 • Rancheria El Municipio, Guerrero • MEXICO

FEI

FEI Number

3010029948

📍

Location

Rancheria El Municipio, Guerrero

🇲🇽

Country

MEXICO
🏢

Address

Calle Calderon Del La Barca 27, Cocula, Rancheria El Municipio, Guerrero, Mexico

Moderate Risk

FDA Import Risk Assessment

32.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
3/12/2013
Latest Refusal
3/12/2013
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
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

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).

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
3/12/2013
60XBY02METOPROLOL (ANTI-ADRENERGIC)
118NOT LISTED
75UNAPPROVED
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Laboratorio Kener Sa De Cv's FDA import refusal history?

Laboratorio Kener Sa De Cv (FEI: 3010029948) has 1 FDA import refusal record(s) in our database, spanning from 3/12/2013 to 3/12/2013.

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. Laboratorio Kener Sa De Cv's FEI number is 3010029948.

What types of violations has Laboratorio Kener Sa De Cv received?

Laboratorio Kener Sa De Cv has been cited for 2 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 Laboratorio Kener Sa De Cv come from?

All FDA import refusal data for Laboratorio Kener Sa De Cv 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.