YDIK NATURE CARE PRODUCTS
⚠️ Moderate Risk
FEI: 3020612037 • Ahmedabad, Gujarat • INDIA
FEI Number
3020612037
Location
Ahmedabad, Gujarat
Country
INDIAAddress
Rambhai Estate, Block # 944, Aslali, Ahmedabad, Gujarat, 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
UNSAFE COL
The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).
DIETARYLBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(s)(2)(B) of the FD&C Act in that the label or labeling fails to identify the product by using the term "dietary supplement", which term may be modified with the name of such an ingredient.
LIST INGRE
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.
NUTRIT LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.
FALSE
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.
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 |
|---|---|---|---|
| 10/25/2021 | 54FYY99HERBALS & BOTANICALS (NOT TEAS), N.E.C. | Division of Northeast Imports (DNEI) | |
| 10/25/2021 | 54KYY10MORINGA OLEIFERA (HERBAL AND BOTANICAL (NOT TEAS II) CONTD | Division of Northeast Imports (DNEI) | |
| 10/25/2021 | 54KYY10MORINGA OLEIFERA (HERBAL AND BOTANICAL (NOT TEAS II) CONTD | Division of Northeast Imports (DNEI) | |
| 10/25/2021 | 54KYY10MORINGA OLEIFERA (HERBAL AND BOTANICAL (NOT TEAS II) CONTD | Division of Northeast Imports (DNEI) | |
| 10/25/2021 | 54KYY10MORINGA OLEIFERA (HERBAL AND BOTANICAL (NOT TEAS II) CONTD | Division of Northeast Imports (DNEI) | |
| 10/25/2021 | 54KYY10MORINGA OLEIFERA (HERBAL AND BOTANICAL (NOT TEAS II) CONTD | Division of Northeast Imports (DNEI) | |
| 10/25/2021 | 54KYY10MORINGA OLEIFERA (HERBAL AND BOTANICAL (NOT TEAS II) CONTD | Division of Northeast Imports (DNEI) | |
| 10/25/2021 | 54KYY10MORINGA OLEIFERA (HERBAL AND BOTANICAL (NOT TEAS II) CONTD | Division of Northeast Imports (DNEI) | |
| 10/25/2021 | 54FYY99HERBALS & BOTANICALS (NOT TEAS), N.E.C. | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is YDIK NATURE CARE PRODUCTS's FDA import refusal history?
YDIK NATURE CARE PRODUCTS (FEI: 3020612037) has 9 FDA import refusal record(s) in our database, spanning from 10/25/2021 to 10/25/2021.
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. YDIK NATURE CARE PRODUCTS's FEI number is 3020612037.
What types of violations has YDIK NATURE CARE PRODUCTS received?
YDIK NATURE CARE PRODUCTS has been cited for 6 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 YDIK NATURE CARE PRODUCTS come from?
All FDA import refusal data for YDIK NATURE CARE PRODUCTS 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.