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Astra Zeneca S.A. de C.V.

⚠️ Moderate Risk

FEI: 3005047667 • Naucalpan de Juarez, Mexico • MEXICO

FEI

FEI Number

3005047667

📍

Location

Naucalpan de Juarez, Mexico

🇲🇽

Country

MEXICO
🏢

Address

Avenida Super Avenida Lomas Verdes No., 67;Fracc. LOMAS VERDES, Naucalpan de Juarez, Mexico, Mexico

Moderate Risk

FDA Import Risk Assessment

45.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
12/13/2011
Latest Refusal
12/7/2011
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
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

753×

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
12/13/2011
64BCB25HYDROCHLOROTHIAZIDE (DIURETIC)
75UNAPPROVED
New Orleans District Office (NOL-DO)
12/7/2011
60QDY07LIDOCAINE
75UNAPPROVED
New Orleans District Office (NOL-DO)
12/7/2011
60QCB07LIDOCAINE
75UNAPPROVED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Astra Zeneca S.A. de C.V.'s FDA import refusal history?

Astra Zeneca S.A. de C.V. (FEI: 3005047667) has 3 FDA import refusal record(s) in our database, spanning from 12/7/2011 to 12/13/2011.

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. Astra Zeneca S.A. de C.V.'s FEI number is 3005047667.

What types of violations has Astra Zeneca S.A. de C.V. received?

Astra Zeneca S.A. de C.V. 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 Astra Zeneca S.A. de C.V. come from?

All FDA import refusal data for Astra Zeneca S.A. de C.V. 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.