Phiha Co Ltd
⚠️ Moderate Risk
FEI: 3006046768 • Hochiminh City • VIETNAM
FEI Number
3006046768
Location
Hochiminh City
Country
VIETNAMAddress
306 Dao Duy Anh, , Hochiminh City, , Vietnam
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
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.
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.
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).
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.
LACKS N/C
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)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.
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).
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)).
TRANSFAT
The product is misbranded under Section 403(q) because the nutrition label does not provide all of the information required by 21 CFR 101.9(c); specifically, the label does not bear the amount of trans fat [21 CFR 101.9(c)(2)(ii)].
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
COLOR LBLG
The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.
FILTHY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 5/11/2009 | 33AGT06FLAVORED CANDY, HARD (LIVE SAVERS, ETC.), WITH NUTS OR NUT PRODUCTS (NOT COCONUT OR SUCKERS)(WITHOUT | 482NUTRIT LBL | Los Angeles District Office (LOS-DO) |
| 5/11/2009 | 07YGT99SNACK FOODS NOT ELSEWHERE MENTIONED, N.E.C. | Los Angeles District Office (LOS-DO) | |
| 5/11/2009 | 21TGT02BANANA, DRIED OR PASTE | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 5/11/2009 | 31KFT01TEA, BLACK | Los Angeles District Office (LOS-DO) | |
| 3/19/2008 | 66VCY99MISCELLANEOUS PATENT MEDICINES, ETC. | 75UNAPPROVED | Los Angeles District Office (LOS-DO) |
| 3/19/2008 | 66VCY99MISCELLANEOUS PATENT MEDICINES, ETC. | 75UNAPPROVED | Los Angeles District Office (LOS-DO) |
| 3/11/2008 | 03YGY99OTHER BAKERY PRODUCTS, N.E.C. | Los Angeles District Office (LOS-DO) | |
| 1/11/2008 | 33AGT06FLAVORED CANDY, HARD (LIVE SAVERS, ETC.), WITH NUTS OR NUT PRODUCTS (NOT COCONUT OR SUCKERS)(WITHOUT | Los Angeles District Office (LOS-DO) | |
| 1/11/2008 | 33AGT12MIXED/ASSORTED HARD CANDIES W/NUT,NUT PRODS,SEEDS W/O COCONUT W/O CHOCOLATE | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Phiha Co Ltd's FDA import refusal history?
Phiha Co Ltd (FEI: 3006046768) has 9 FDA import refusal record(s) in our database, spanning from 1/11/2008 to 5/11/2009.
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. Phiha Co Ltd's FEI number is 3006046768.
What types of violations has Phiha Co Ltd received?
Phiha Co Ltd 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 Phiha Co Ltd come from?
All FDA import refusal data for Phiha Co 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.