Advaita Pharmaceuticals
⚠️ High Risk
FEI: 3012123333 • Ciudad De Mexico, Ciudad de Mexico • MEXICO
FEI Number
3012123333
Location
Ciudad De Mexico, Ciudad de Mexico
Country
MEXICOAddress
Calle Adolfo Prieto # 1427, Otro Tlacoquemecatl Del Valle, Benito Juarez, Ciudad De Mexico, Ciudad de Mexico, Mexico
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
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 |
|---|---|---|---|
| 11/22/2023 | 64XDY11ISOTRETINOIN (KERATOLYTIC) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 4/20/2023 | 56EDA60MINOCYCLINE (TETRACYCLINES) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 12/7/2022 | 64XCY11ISOTRETINOIN (KERATOLYTIC) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 6/5/2020 | 64XCY11ISOTRETINOIN (KERATOLYTIC) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is Advaita Pharmaceuticals's FDA import refusal history?
Advaita Pharmaceuticals (FEI: 3012123333) has 4 FDA import refusal record(s) in our database, spanning from 6/5/2020 to 11/22/2023.
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. Advaita Pharmaceuticals's FEI number is 3012123333.
What types of violations has Advaita Pharmaceuticals received?
Advaita Pharmaceuticals 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 Advaita Pharmaceuticals come from?
All FDA import refusal data for Advaita Pharmaceuticals 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.