Philips Medical Systems Technologies Ltd
⚠️ Moderate Risk
FEI: 3008581796 • Haifa • ISRAEL
FEI Number
3008581796
Location
Haifa
Country
ISRAELAddress
Building 34, Advanced Technology Center Matam, Haifa, , Israel
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
NO REGISTR
The article appears to be an electronic product that does not comply with an applicable standard as prescribed by Section 534 because no reporting has been provided as required by Section 537(b).
NON STD
The article is subject to refusal of admission pursuant to section 536(a) of the Federal Food, Drug, and Cosmetic Act (FFDCA) in that it appears to be an electronic product offered for importation into the United States which fails to comply with an applicable standard prescribed pursuant to section 534 of the FFDCA.
Refusal History
Frequently Asked Questions
What is Philips Medical Systems Technologies Ltd's FDA import refusal history?
Philips Medical Systems Technologies Ltd (FEI: 3008581796) has 2 FDA import refusal record(s) in our database, spanning from 3/31/2003 to 6/13/2003.
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. Philips Medical Systems Technologies Ltd's FEI number is 3008581796.
What types of violations has Philips Medical Systems Technologies Ltd received?
Philips Medical Systems Technologies Ltd 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 Philips Medical Systems Technologies Ltd come from?
All FDA import refusal data for Philips Medical Systems Technologies Ltd 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.