Grand Imports & Exports
⚠️ Moderate Risk
FEI: 3004957015 • Faoshan, Guangdong • CHINA
FEI Number
3004957015
Location
Faoshan, Guangdong
Country
CHINAAddress
7/F Rifeng Bldg., 16 Zumiao Road, , Faoshan, Guangdong, China
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
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.
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).
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.
DRUG NAME
The article appears to be a drug and fails to bear the proprietary or established name and/or name and quantity of each active ingredient.
POISONOUS
The article is subject to refusal of admission pursuant Section 801(a)(3) in that The cosmetic appears to bear or contain a poisonous or deleterious substance which may render it injurious to users under the conditions prescribed in the labeling thereof, or, under such conditions of use as are customary or usual.
INCONSPICU
Information required by the Act to be on the label or labeling does not appear to be conspicuous enough as to render it likely to be read and understood by the ordinary individual under customary conditions of purchase and use.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/10/2007 | 53LY03FACE,BODY,AND HAND (EXCLUDING SHAVING PREPARATIONS) (SKIN CARE PREPARATIONS) | New York District Office (NYK-DO) | |
| 12/10/2007 | 53JY99OTHER PERSONAL CLEANLINESS PRODUCTS (NOT ANTIPERSPIRANT), N.E.C. | New York District Office (NYK-DO) | |
| 6/12/2007 | 61HBY99ANTI-BACTERIAL, N.E.C. | New York District Office (NYK-DO) | |
| 6/12/2007 | 61HBY99ANTI-BACTERIAL, N.E.C. | New York District Office (NYK-DO) | |
| 6/12/2007 | 61HBY99ANTI-BACTERIAL, N.E.C. | 118NOT LISTED | New York District Office (NYK-DO) |
| 5/3/2007 | 61HBY99ANTI-BACTERIAL, N.E.C. | New York District Office (NYK-DO) | |
| 9/13/2006 | 53LF01CLEANSING (COLD CREAMS, CLEANSING LOTIONS, LIQUIDS, PADS) (SKIN CARE PREPARATIONS) | 471CSTIC LBLG | New York District Office (NYK-DO) |
| 7/21/2006 | 61HBY99ANTI-BACTERIAL, N.E.C. | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Grand Imports & Exports's FDA import refusal history?
Grand Imports & Exports (FEI: 3004957015) has 8 FDA import refusal record(s) in our database, spanning from 7/21/2006 to 12/10/2007.
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. Grand Imports & Exports's FEI number is 3004957015.
What types of violations has Grand Imports & Exports received?
Grand Imports & Exports 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 Grand Imports & Exports come from?
All FDA import refusal data for Grand Imports & Exports 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.