ImportRefusal LogoImportRefusal

Rebeca Hernandes

⚠️ Moderate Risk

FEI: 3003840101 • Mexico City • MEXICO

FEI

FEI Number

3003840101

📍

Location

Mexico City

🇲🇽

Country

MEXICO
🏢

Address

Sto. Domingo No 55, , Mexico City, , Mexico

Moderate Risk

FDA Import Risk Assessment

41.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
2
Unique Violations
1/21/2003
Latest Refusal
1/21/2003
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

752×

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).

1791×

AGR RX

The article appears to be a prescription drug manufactured in the U.S. and offered for import by other than the manufacturer and reimportation does not appear to have been authorized by the Secretary for use in a medical emergency.

Refusal History

DateProductViolationsDivision
1/21/2003
56YCY99ANTIBIOTIC N.E.C.
179AGR RX
New Orleans District Office (NOL-DO)
1/21/2003
56YCY99ANTIBIOTIC N.E.C.
75UNAPPROVED
New Orleans District Office (NOL-DO)
1/21/2003
56YCY99ANTIBIOTIC N.E.C.
75UNAPPROVED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Rebeca Hernandes's FDA import refusal history?

Rebeca Hernandes (FEI: 3003840101) has 3 FDA import refusal record(s) in our database, spanning from 1/21/2003 to 1/21/2003.

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. Rebeca Hernandes's FEI number is 3003840101.

What types of violations has Rebeca Hernandes received?

Rebeca Hernandes 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 Rebeca Hernandes come from?

All FDA import refusal data for Rebeca Hernandes 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.