Laboratorio Pablo Cassara
⚠️ Moderate Risk
FEI: 3005721395 • Ciudad Autonoma Buenos Aires, Capital Federal • ARGENTINA
FEI Number
3005721395
Location
Ciudad Autonoma Buenos Aires, Capital Federal
Country
ARGENTINAAddress
Calle Carhue 1096, , Ciudad Autonoma Buenos Aires, Capital Federal, Argentina
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
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
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 |
|---|---|---|---|
| 1/7/2013 | 66YIK99EXHIBITS - OTHER DRUG RELATED ITEMS N.E.C. | 75UNAPPROVED | Florida District Office (FLA-DO) |
| 11/23/2012 | 66YIK99EXHIBITS - OTHER DRUG RELATED ITEMS N.E.C. | 118NOT LISTED | Florida District Office (FLA-DO) |
| 6/5/2012 | 66YIK99EXHIBITS - OTHER DRUG RELATED ITEMS N.E.C. | 118NOT LISTED | Florida District Office (FLA-DO) |
Frequently Asked Questions
What is Laboratorio Pablo Cassara's FDA import refusal history?
Laboratorio Pablo Cassara (FEI: 3005721395) has 3 FDA import refusal record(s) in our database, spanning from 6/5/2012 to 1/7/2013.
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. Laboratorio Pablo Cassara's FEI number is 3005721395.
What types of violations has Laboratorio Pablo Cassara received?
Laboratorio Pablo Cassara has been cited for 2 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 Laboratorio Pablo Cassara come from?
All FDA import refusal data for Laboratorio Pablo Cassara 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.