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ANA LILIA SAENZ ACOSTA

⚠️ Moderate Risk

FEI: 3016404639 • Pachuca • MEXICO

FEI

FEI Number

3016404639

📍

Location

Pachuca

🇲🇽

Country

MEXICO
🏢

Address

Blvd. Luis Donaldo Colosio # 2009, , Pachuca, , Mexico

Moderate Risk

FDA Import Risk Assessment

30.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
2/12/2020
Latest Refusal
2/12/2020
Earliest Refusal

Score Breakdown

Violation Severity
65.0×40%
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

3361×

INCONSPICU

Information required by the Act to be on the label or labeling does not appear to be conspicuous enough as to render it likely to be read and understood by the ordinary individual under customary conditions of purchase and use.

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
2/12/2020
66VCA99MISCELLANEOUS PATENT MEDICINES, ETC.
336INCONSPICU
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is ANA LILIA SAENZ ACOSTA's FDA import refusal history?

ANA LILIA SAENZ ACOSTA (FEI: 3016404639) has 1 FDA import refusal record(s) in our database, spanning from 2/12/2020 to 2/12/2020.

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 LILIA SAENZ ACOSTA's FEI number is 3016404639.

What types of violations has ANA LILIA SAENZ ACOSTA received?

ANA LILIA SAENZ ACOSTA 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 ANA LILIA SAENZ ACOSTA come from?

All FDA import refusal data for ANA LILIA SAENZ ACOSTA 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.