ImportRefusal LogoImportRefusal

Laboratorios Cidest

⚠️ Moderate Risk

FEI: 2000033609 • Ciudad General Escobedo, Nuevo Leon • MEXICO

FEI

FEI Number

2000033609

📍

Location

Ciudad General Escobedo, Nuevo Leon

🇲🇽

Country

MEXICO
🏢

Address

Calle Lazaro Cardenas 801, Col. Los Altos, Gral. Escobedo, Ciudad General Escobedo, Nuevo Leon, Mexico

Moderate Risk

FDA Import Risk Assessment

43.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
6/21/2011
Latest Refusal
6/21/2011
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
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

3082×

MFR INSAN

The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.

Refusal History

DateProductViolationsDivision
6/21/2011
16AGH99FISH, N.E.C.
308MFR INSAN
Southwest Import District Office (SWI-DO)
6/21/2011
16AGH99FISH, N.E.C.
308MFR INSAN
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Laboratorios Cidest's FDA import refusal history?

Laboratorios Cidest (FEI: 2000033609) has 2 FDA import refusal record(s) in our database, spanning from 6/21/2011 to 6/21/2011.

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. Laboratorios Cidest's FEI number is 2000033609.

What types of violations has Laboratorios Cidest received?

Laboratorios Cidest 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 Laboratorios Cidest come from?

All FDA import refusal data for Laboratorios Cidest 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.