Guangzhou Fu Bao Daily Chemical Co.,Ltd.
⚠️ High Risk
FEI: 3012631848 • Guangzhou, Guangdong • CHINA
FEI Number
3012631848
Location
Guangzhou, Guangdong
Country
CHINAAddress
B Building, 51 North Zhenhua Road; Shenshan Industrial Estate, Guangzhou, Guangdong, China
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
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
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).
DIRSEXMPT
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a drug within the meaning of Section 201(g) and it lacks adequate directions for use.
FRNMFGREG
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.
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).
LACKS FIRM
The article is in package form and appears to not bear a label containing the name and place of business of the manufacturer, packer, or distributor.
LACKS N/C
The article is in package form and appears to not have a label containing an accurate statement of the quantity of the contents in terms of weight, measure or numerical count and no variations or exemptions have been prescribed by regs.
N-RX INACT
The article appears to be a nonprescription drug and fails to bear the established name of each inactive ingredient in alphabetical order on the outside container of the retail package.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/15/2025 | 53LC06MOISTURIZING (SKIN CARE PREPARATIONS) | 75UNAPPROVED | Division of Northern Border Imports (DNBI) |
| 5/3/2021 | 53LD06MOISTURIZING (SKIN CARE PREPARATIONS) | 3280FRNMFGREG | Division of West Coast Imports (DWCI) |
| 5/16/2019 | 62GBJ99ANTI-INFLAMMATORY N.E.C. | Division of Southeast Imports (DSEI) | |
| 12/7/2016 | 66VCY99MISCELLANEOUS PATENT MEDICINES, ETC. | New York District Office (NYK-DO) | |
| 12/7/2016 | 66VCY99MISCELLANEOUS PATENT MEDICINES, ETC. | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Guangzhou Fu Bao Daily Chemical Co.,Ltd.'s FDA import refusal history?
Guangzhou Fu Bao Daily Chemical Co.,Ltd. (FEI: 3012631848) has 5 FDA import refusal record(s) in our database, spanning from 12/7/2016 to 12/15/2025.
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. Guangzhou Fu Bao Daily Chemical Co.,Ltd.'s FEI number is 3012631848.
What types of violations has Guangzhou Fu Bao Daily Chemical Co.,Ltd. received?
Guangzhou Fu Bao Daily Chemical Co.,Ltd. has been cited for 7 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 Guangzhou Fu Bao Daily Chemical Co.,Ltd. come from?
All FDA import refusal data for Guangzhou Fu Bao Daily Chemical 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.