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BEVI ASIA PACIFIC INC

⚠️ Moderate Risk

FEI: 3013585693 • Makati, National Capital Region • PHILIPPINES

FEI

FEI Number

3013585693

📍

Location

Makati, National Capital Region

🇵🇭
🏢

Address

3/F 1262 Batangas Street, Corner of Honduras Street, San Isidro, Makati, National Capital Region, Philippines

Moderate Risk

FDA Import Risk Assessment

49.0
LowModerateHighCritical

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

Statistics

23
Total Refusals
6
Unique Violations
2/13/2018
Latest Refusal
11/20/2012
Earliest Refusal

Score Breakdown

Violation Severity
73.3×40%
Refusal Volume
51.1×30%
Recency
0.0×20%
Frequency
43.9×10%
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

7521×

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).

11813×

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).

164×

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.

1783×

COL ADDED

The article appears to bear or contain, for the purpose of coloring only, a color additive which is unsafe within the meaning of Section 721(a).

3301×

UNSAFE COL

The article appears to be a color additive for the purposes of coloring only in or on drugs or devices, and is unsafe within the meaning of Section 721(a).

4711×

CSTIC LBLG

The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.

Refusal History

DateProductViolationsDivision
2/13/2018
53LY99OTHER SKIN CARE PREPARATIONS, N.E.C.
75UNAPPROVED
Division of Southwest Imports (DSWI)
2/13/2018
53LY99OTHER SKIN CARE PREPARATIONS, N.E.C.
75UNAPPROVED
Division of Southwest Imports (DSWI)
2/13/2018
53LY99OTHER SKIN CARE PREPARATIONS, N.E.C.
75UNAPPROVED
Division of Southwest Imports (DSWI)
2/13/2018
53LY99OTHER SKIN CARE PREPARATIONS, N.E.C.
75UNAPPROVED
Division of Southwest Imports (DSWI)
2/13/2018
53LY99OTHER SKIN CARE PREPARATIONS, N.E.C.
75UNAPPROVED
Division of Southwest Imports (DSWI)
12/18/2012
53JD01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS)
471CSTIC LBLG
San Francisco District Office (SAN-DO)
12/18/2012
66VBL99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
178COL ADDED
75UNAPPROVED
San Francisco District Office (SAN-DO)
12/18/2012
66VBL99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
178COL ADDED
75UNAPPROVED
San Francisco District Office (SAN-DO)
12/18/2012
66VBU99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
75UNAPPROVED
San Francisco District Office (SAN-DO)
12/18/2012
66VBU99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
75UNAPPROVED
San Francisco District Office (SAN-DO)
12/18/2012
66VBU99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
75UNAPPROVED
San Francisco District Office (SAN-DO)
12/18/2012
66VBU99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
75UNAPPROVED
San Francisco District Office (SAN-DO)
12/18/2012
66VBL99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
75UNAPPROVED
San Francisco District Office (SAN-DO)
12/18/2012
66VBL99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
75UNAPPROVED
San Francisco District Office (SAN-DO)
12/18/2012
66VBL99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
16DIRECTIONS
330UNSAFE COL
75UNAPPROVED
San Francisco District Office (SAN-DO)
12/18/2012
66VBL99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
16DIRECTIONS
178COL ADDED
75UNAPPROVED
San Francisco District Office (SAN-DO)
12/18/2012
66VBJ99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
16DIRECTIONS
75UNAPPROVED
San Francisco District Office (SAN-DO)
12/18/2012
66VBJ99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
16DIRECTIONS
75UNAPPROVED
San Francisco District Office (SAN-DO)
12/18/2012
66PBJ99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C.
118NOT LISTED
San Francisco District Office (SAN-DO)
11/20/2012
53JD01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS)
75UNAPPROVED
Los Angeles District Office (LOS-DO)
11/20/2012
53JD01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS)
75UNAPPROVED
Los Angeles District Office (LOS-DO)
11/20/2012
53JD01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS)
75UNAPPROVED
Los Angeles District Office (LOS-DO)
11/20/2012
53JD01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS)
75UNAPPROVED
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is BEVI ASIA PACIFIC INC's FDA import refusal history?

BEVI ASIA PACIFIC INC (FEI: 3013585693) has 23 FDA import refusal record(s) in our database, spanning from 11/20/2012 to 2/13/2018.

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. BEVI ASIA PACIFIC INC's FEI number is 3013585693.

What types of violations has BEVI ASIA PACIFIC INC received?

BEVI ASIA PACIFIC INC 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 BEVI ASIA PACIFIC INC come from?

All FDA import refusal data for BEVI ASIA PACIFIC 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.