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HAIDEE GARCIA

⚠️ Moderate Risk

FEI: 3018067807 • Jojutla, Morelos • MEXICO

FEI

FEI Number

3018067807

📍

Location

Jojutla, Morelos

🇲🇽

Country

MEXICO
🏢

Address

Avenida Altamirano 222, Barrio Centro, Jojutla, Jojutla, Morelos, Mexico

Moderate Risk

FDA Import Risk Assessment

47.8
LowModerateHighCritical

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

Statistics

4
Total Refusals
1
Unique Violations
5/6/2021
Latest Refusal
5/6/2021
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
40.0×10%
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

754×

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
5/6/2021
56CYY27CEPHALEXIN (CEPHALOSPORINS)
75UNAPPROVED
Division of Southeast Imports (DSEI)
5/6/2021
62VCY45OSELTAMIVIR PHOSPHATE (ANTI-VIRAL)
75UNAPPROVED
Division of Southeast Imports (DSEI)
5/6/2021
56YYY99ANTIBIOTIC N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)
5/6/2021
62UDY08CODEINE PHOSPHATE (ANTI-TUSSIVE/COLD)
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is HAIDEE GARCIA's FDA import refusal history?

HAIDEE GARCIA (FEI: 3018067807) has 4 FDA import refusal record(s) in our database, spanning from 5/6/2021 to 5/6/2021.

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. HAIDEE GARCIA's FEI number is 3018067807.

What types of violations has HAIDEE GARCIA received?

HAIDEE GARCIA 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 HAIDEE GARCIA come from?

All FDA import refusal data for HAIDEE GARCIA 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.