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Candida Mejia

⚠️ Moderate Risk

FEI: 3005938907 • Actopan • MEXICO

FEI

FEI Number

3005938907

📍

Location

Actopan

🇲🇽

Country

MEXICO
🏢

Address

Unknown Street, , Actopan, , Mexico

Moderate Risk

FDA Import Risk Assessment

25.7
LowModerateHighCritical

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

Statistics

1
Total Refusals
3
Unique Violations
10/16/2006
Latest Refusal
10/16/2006
Earliest Refusal

Score Breakdown

Violation Severity
53.3×40%
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

1151×

DR QUALITY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to be represented as a drug the name of which is recognized in an official compendium and its strength appears to differ from or its quality or purity appear to fall below the standards set forth in such compendium.

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

3331×

LACKS FIRM

The article is in package form and appears to not bear a label containing the name and place of business of the manufacturer, packer, or distributor.

Refusal History

DateProductViolationsDivision
10/16/2006
66VBY99MISCELLANEOUS PATENT MEDICINES, ETC.
115DR QUALITY
16DIRECTIONS
333LACKS FIRM
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Candida Mejia's FDA import refusal history?

Candida Mejia (FEI: 3005938907) has 1 FDA import refusal record(s) in our database, spanning from 10/16/2006 to 10/16/2006.

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. Candida Mejia's FEI number is 3005938907.

What types of violations has Candida Mejia received?

Candida Mejia has been cited for 3 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 Candida Mejia come from?

All FDA import refusal data for Candida Mejia 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.