Nidaria Technology, LTD.
⚠️ Moderate Risk
FEI: 3003052101 • Jordan Valley • ISRAEL
FEI Number
3003052101
Location
Jordan Valley
Country
ISRAELAddress
Zemach, , Jordan Valley, , 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
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/1/2011 | 65LBL99PROTECTANT N.E.C. | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 12/1/2011 | 65LBL99PROTECTANT N.E.C. | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 12/1/2011 | 65LBL11TITANIUM DIOXIDE (PROTECTANT) | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 7/2/2008 | 66PBL99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C. | 118NOT LISTED | New York District Office (NYK-DO) |
| 7/2/2008 | 66PBL99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C. | 118NOT LISTED | New York District Office (NYK-DO) |
| 7/2/2008 | 66PBL99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C. | 118NOT LISTED | New York District Office (NYK-DO) |
| 7/2/2008 | 66PBL99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C. | 118NOT LISTED | New York District Office (NYK-DO) |
| 7/2/2008 | 66PBL99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C. | 118NOT LISTED | New York District Office (NYK-DO) |
| 5/19/2005 | 53MD01SUNTAN GELS, CREAMS, LIQUIDS (NOT SUNSCREEN) (SUNTAN PREPARATIONS) | 118NOT LISTED | New York District Office (NYK-DO) |
| 5/19/2005 | 53MD01SUNTAN GELS, CREAMS, LIQUIDS (NOT SUNSCREEN) (SUNTAN PREPARATIONS) | 118NOT LISTED | New York District Office (NYK-DO) |
| 5/19/2005 | 53MD01SUNTAN GELS, CREAMS, LIQUIDS (NOT SUNSCREEN) (SUNTAN PREPARATIONS) | 118NOT LISTED | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Nidaria Technology, LTD.'s FDA import refusal history?
Nidaria Technology, LTD. (FEI: 3003052101) has 11 FDA import refusal record(s) in our database, spanning from 5/19/2005 to 12/1/2011.
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. Nidaria Technology, LTD.'s FEI number is 3003052101.
What types of violations has Nidaria Technology, LTD. received?
Nidaria Technology, LTD. 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 Nidaria Technology, LTD. come from?
All FDA import refusal data for Nidaria Technology, 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.