Directiva Sa De Cv
✅ Low Risk
FEI: 3005805183 • Df • MEXICO
FEI Number
3005805183
Location
Df
Country
MEXICOAddress
Toltecas 27, Col Barrio De Santa Barabara, Df, , Mexico
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity 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
REGISTERED
It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/16/2006 | 89ISAMASSAGER, THERAPEUTIC, ELECTRIC | 341REGISTERED | Florida District Office (FLA-DO) |
Frequently Asked Questions
What is Directiva Sa De Cv's FDA import refusal history?
Directiva Sa De Cv (FEI: 3005805183) has 1 FDA import refusal record(s) in our database, spanning from 10/16/2006 to 10/16/2006.
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. Directiva Sa De Cv's FEI number is 3005805183.
What types of violations has Directiva Sa De Cv received?
Directiva Sa De Cv 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 Directiva Sa De Cv come from?
All FDA import refusal data for Directiva Sa De Cv 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.