ASTRAZENECA SA
⚠️ Moderate Risk
FEI: 3012742529 • Naucalpan de Ju • MEXICO
FEI Number
3012742529
Location
Naucalpan de Ju
Country
MEXICOAddress
Super Avenida Lomas Ver, , Naucalpan de Ju, , Mexico
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/18/2020 | 66VCA99MISCELLANEOUS PATENT MEDICINES, ETC. | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 6/15/2020 | 62ODA19CANDESARTAN CILEXETIL (ANTI-HYPERTENSIVE - PART II) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 1/16/2019 | 61JCB16ROSUVASTATIN CALCIUM | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 12/22/2017 | 61UDA05TAMOXIFEN CITRATE (ANTI-ESTROGEN) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 4/5/2017 | 60LDA17CLONIXIN (ANALGESIC) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is ASTRAZENECA SA's FDA import refusal history?
ASTRAZENECA SA (FEI: 3012742529) has 5 FDA import refusal record(s) in our database, spanning from 4/5/2017 to 9/18/2020.
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. ASTRAZENECA SA's FEI number is 3012742529.
What types of violations has ASTRAZENECA SA received?
ASTRAZENECA SA 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 ASTRAZENECA SA come from?
All FDA import refusal data for ASTRAZENECA SA 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.