CENTER PHYTOCHAI
⚠️ Moderate Risk
FEI: 3013727200 • Solnechnogorsk, Moskovskaya obl • RUSSIA
FEI Number
3013727200
Location
Solnechnogorsk, Moskovskaya obl
Country
RUSSIAAddress
Ul. Lva Tolstogo 42, , Solnechnogorsk, Moskovskaya obl, Russia
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
DIRECTIONS
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.
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.
COLOR LBLG
The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.
LACKS FIRM
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(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.
NO ENGLISH
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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).
ALLERGEN
the label fails to declare all major food allergens present in the product, as required by section 403(w)(1).
DIETARYING
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)(A) of the FD&C Act in that the dietary supplement label or labeling fails to list the name of each dietary ingredient of the supplement and the quantity of each such dietary ingredient or , with respect to a proprietary blend of such dietary ingredients, the total quantity of all dietary ingredients in the blend.
PLANT PART
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)(C) of the FD&C Act in that the supplement contains an herb or other botanical described in section 201(ff)(1)(C), and the label or labeling of the supplement fails to identify any part of the plant from which the ingredient is derived.
NCONTACT
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(y) of the FD&C Act in that the dietary supplement label fails to bear a domestic address or phone number through which the responsible person (as described in section 761 of the FD&C Act) may receive a report of a serious adverse event with such dietary supplement.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/9/2017 | 54ECT99HERBALS & BOTANICAL TEAS, N.E.C. | Division of Northern Border Imports (DNBI) | |
| 11/9/2017 | 54ECT99HERBALS & BOTANICAL TEAS, N.E.C. | Division of Northern Border Imports (DNBI) | |
| 11/9/2017 | 54ECT99HERBALS & BOTANICAL TEAS, N.E.C. | Division of Northern Border Imports (DNBI) | |
| 11/9/2017 | 54ECT99HERBALS & BOTANICAL TEAS, N.E.C. | Division of Northern Border Imports (DNBI) | |
| 11/9/2017 | 54ECT99HERBALS & BOTANICAL TEAS, N.E.C. | Division of Northern Border Imports (DNBI) | |
| 11/9/2017 | 54ECT99HERBALS & BOTANICAL TEAS, N.E.C. | Division of Northern Border Imports (DNBI) | |
| 11/9/2017 | 54ECT99HERBALS & BOTANICAL TEAS, N.E.C. | Division of Northern Border Imports (DNBI) | |
| 11/9/2017 | 54ECT99HERBALS & BOTANICAL TEAS, N.E.C. | Division of Northern Border Imports (DNBI) | |
| 11/9/2017 | 54ECT99HERBALS & BOTANICAL TEAS, N.E.C. | Division of Northern Border Imports (DNBI) | |
| 11/9/2017 | 54ECT99HERBALS & BOTANICAL TEAS, N.E.C. | Division of Northern Border Imports (DNBI) | |
| 11/9/2017 | 54ECT99HERBALS & BOTANICAL TEAS, N.E.C. | Division of Northern Border Imports (DNBI) |
Frequently Asked Questions
What is CENTER PHYTOCHAI's FDA import refusal history?
CENTER PHYTOCHAI (FEI: 3013727200) has 11 FDA import refusal record(s) in our database, spanning from 11/9/2017 to 11/9/2017.
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. CENTER PHYTOCHAI's FEI number is 3013727200.
What types of violations has CENTER PHYTOCHAI received?
CENTER PHYTOCHAI has been cited for 11 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 CENTER PHYTOCHAI come from?
All FDA import refusal data for CENTER PHYTOCHAI 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.