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Padilla Gabriela P Srita

⚠️ Moderate Risk

FEI: 3004415705 • Col Centro Piso • MEXICO

FEI

FEI Number

3004415705

📍

Location

Col Centro Piso

🇲🇽

Country

MEXICO
🏢

Address

Av Fray Servando T De Mier 356, , Col Centro Piso, , 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
2/25/2004
Latest Refusal
2/25/2004
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

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).

Refusal History

DateProductViolationsDivision
2/25/2004
61NCB65CITALOPRAM HYDROBROMIDE (ANTI-DEPRESSANT)
75UNAPPROVED
New Orleans District Office (NOL-DO)
2/25/2004
63XIS99DIAGOSTIC AID (DRUGS) N.E.C.
75UNAPPROVED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Padilla Gabriela P Srita's FDA import refusal history?

Padilla Gabriela P Srita (FEI: 3004415705) has 2 FDA import refusal record(s) in our database, spanning from 2/25/2004 to 2/25/2004.

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. Padilla Gabriela P Srita's FEI number is 3004415705.

What types of violations has Padilla Gabriela P Srita received?

Padilla Gabriela P Srita 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 Padilla Gabriela P Srita come from?

All FDA import refusal data for Padilla Gabriela P Srita 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.