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Phiha Co Ltd

⚠️ Moderate Risk

FEI: 3006046768 • Hochiminh City • VIETNAM

FEI

FEI Number

3006046768

📍

Location

Hochiminh City

🇻🇳

Country

VIETNAM
🏢

Address

306 Dao Duy Anh, , Hochiminh City, , Vietnam

Moderate Risk

FDA Import Risk Assessment

37.3
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

9
Total Refusals
11
Unique Violations
5/11/2009
Latest Refusal
1/11/2008
Earliest Refusal

Score Breakdown

Violation Severity
48.5×40%
Refusal Volume
37.0×30%
Recency
0.0×20%
Frequency
67.6×10%
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

4825×

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.

2183×

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.

752×

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).

3202×

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.

3212×

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.

111×

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).

3241×

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)).

33201×

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)].

4731×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

2741×

COLOR LBLG

The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.

2491×

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

DateProductViolationsDivision
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.
473LABELING
482NUTRIT LBL
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
218LIST INGRE
320LACKS FIRM
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.
11UNSAFE COL
218LIST INGRE
274COLOR LBLG
320LACKS FIRM
321LACKS N/C
3320TRANSFAT
482NUTRIT LBL
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
321LACKS N/C
324NO ENGLISH
482NUTRIT LBL
Los Angeles District Office (LOS-DO)
1/11/2008
33AGT12MIXED/ASSORTED HARD CANDIES W/NUT,NUT PRODS,SEEDS W/O COCONUT W/O CHOCOLATE
218LIST INGRE
482NUTRIT LBL
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.