ImportRefusal LogoImportRefusal

ANA DIRA

⚠️ Moderate Risk

FEI: 3021542412 • Zapopan • MEXICO

FEI

FEI Number

3021542412

📍

Location

Zapopan

🇲🇽

Country

MEXICO
🏢

Address

Priv Benustraro Cerronz, , Zapopan, , Mexico

Moderate Risk

FDA Import Risk Assessment

27.6
LowModerateHighCritical

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

Statistics

1
Total Refusals
3
Unique Violations
3/21/2022
Latest Refusal
3/21/2022
Earliest Refusal

Score Breakdown

Violation Severity
53.3×40%
Refusal Volume
11.2×30%
Recency
9.7×20%
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

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.

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.

Refusal History

DateProductViolationsDivision
3/21/2022
83QLWCOVID-19 TEST HOME COLLECTION KIT DEVICES
16DIRECTIONS
333LACKS FIRM
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is ANA DIRA's FDA import refusal history?

ANA DIRA (FEI: 3021542412) has 1 FDA import refusal record(s) in our database, spanning from 3/21/2022 to 3/21/2022.

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. ANA DIRA's FEI number is 3021542412.

What types of violations has ANA DIRA received?

ANA DIRA 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 ANA DIRA come from?

All FDA import refusal data for ANA DIRA 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.