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Lite Xpress Intl Inc

⚠️ High Risk

FEI: 3009628463 • Quezon • PHILIPPINES

FEI

FEI Number

3009628463

📍

Location

Quezon

🇵🇭
🏢

Address

Nit 108 Gf The Block, , Quezon, , Philippines

High Risk

FDA Import Risk Assessment

51.2
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

12
Total Refusals
5
Unique Violations
3/2/2015
Latest Refusal
3/2/2015
Earliest Refusal

Score Breakdown

Violation Severity
72.1×40%
Refusal Volume
41.3×30%
Recency
0.0×20%
Frequency
100.0×10%
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

759×

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).

4732×

LABELING

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

1181×

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).

3201×

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.

4821×

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

DateProductViolationsDivision
3/2/2015
54FYS99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
473LABELING
482NUTRIT LBL
Los Angeles District Office (LOS-DO)
3/2/2015
54ACR99VITAMIN, N.E.C.
320LACKS FIRM
473LABELING
Los Angeles District Office (LOS-DO)
3/2/2015
54ACR99VITAMIN, N.E.C.
118NOT LISTED
Los Angeles District Office (LOS-DO)
3/2/2015
53JF01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS)
75UNAPPROVED
Los Angeles District Office (LOS-DO)
3/2/2015
53JF01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS)
75UNAPPROVED
Los Angeles District Office (LOS-DO)
3/2/2015
53JF01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS)
75UNAPPROVED
Los Angeles District Office (LOS-DO)
3/2/2015
53LD03FACE,BODY,AND HAND (EXCLUDING SHAVING PREPARATIONS) (SKIN CARE PREPARATIONS)
75UNAPPROVED
Los Angeles District Office (LOS-DO)
3/2/2015
53LD03FACE,BODY,AND HAND (EXCLUDING SHAVING PREPARATIONS) (SKIN CARE PREPARATIONS)
75UNAPPROVED
Los Angeles District Office (LOS-DO)
3/2/2015
53LD06MOISTURIZING (SKIN CARE PREPARATIONS)
75UNAPPROVED
Los Angeles District Office (LOS-DO)
3/2/2015
53LG08PASTE MASKS (MUD PACKS) (SKIN CARE PREPARATIONS)
75UNAPPROVED
Los Angeles District Office (LOS-DO)
3/2/2015
53JD02DEODORANTS (UNDERARM)(NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS)
75UNAPPROVED
Los Angeles District Office (LOS-DO)
3/2/2015
54ACR99VITAMIN, N.E.C.
75UNAPPROVED
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Lite Xpress Intl Inc's FDA import refusal history?

Lite Xpress Intl Inc (FEI: 3009628463) has 12 FDA import refusal record(s) in our database, spanning from 3/2/2015 to 3/2/2015.

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. Lite Xpress Intl Inc's FEI number is 3009628463.

What types of violations has Lite Xpress Intl Inc received?

Lite Xpress Intl Inc has been cited for 5 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 Lite Xpress Intl Inc come from?

All FDA import refusal data for Lite Xpress Intl Inc 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.