Shriji Herbal Product
⚠️ Moderate Risk
FEI: 3002923929 • Idar, GJ • INDIA
FEI Number
3002923929
Location
Idar, GJ
Country
INDIAAddress
Krishna Nagar, Po Netramli, , Idar, GJ, India
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).
FALSE
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose labeling appears to be false or misleading.
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 |
|---|---|---|---|
| 10/23/2013 | 66VBY99MISCELLANEOUS PATENT MEDICINES, ETC. | New York District Office (NYK-DO) | |
| 11/25/2011 | 54FAT99HERBALS & BOTANICALS (NOT TEAS), N.E.C. | 118NOT LISTED | New York District Office (NYK-DO) |
| 11/25/2011 | 54FAT99HERBALS & BOTANICALS (NOT TEAS), N.E.C. | 118NOT LISTED | New York District Office (NYK-DO) |
| 11/25/2011 | 54FAT99HERBALS & BOTANICALS (NOT TEAS), N.E.C. | 118NOT LISTED | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Shriji Herbal Product's FDA import refusal history?
Shriji Herbal Product (FEI: 3002923929) has 4 FDA import refusal record(s) in our database, spanning from 11/25/2011 to 10/23/2013.
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. Shriji Herbal Product's FEI number is 3002923929.
What types of violations has Shriji Herbal Product received?
Shriji Herbal Product 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 Shriji Herbal Product come from?
All FDA import refusal data for Shriji Herbal Product 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.