LANIFEMS DE RL DE CV
⚠️ Moderate Risk
FEI: 3029983692 • San Luis Potosi, San Luis Potosi • MEXICO
FEI Number
3029983692
Location
San Luis Potosi, San Luis Potosi
Country
MEXICOAddress
Calle Loma Azul 233, Col. Loma Dorada, San Luis Potosi, San Luis Potosi, San Luis Potosi, 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
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).
FRNMFGREG
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.
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
Frequently Asked Questions
What is LANIFEMS DE RL DE CV's FDA import refusal history?
LANIFEMS DE RL DE CV (FEI: 3029983692) has 1 FDA import refusal record(s) in our database, spanning from 12/29/2023 to 12/29/2023.
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. LANIFEMS DE RL DE CV's FEI number is 3029983692.
What types of violations has LANIFEMS DE RL DE CV received?
LANIFEMS DE RL DE CV has been cited for 3 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 LANIFEMS DE RL DE CV come from?
All FDA import refusal data for LANIFEMS DE RL 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.