Ming Fai Industrial (Shenzhen) Co LTD
⚠️ High Risk
FEI: 3003340745 • Shenzhen, Guangdong • CHINA
FEI Number
3003340745
Location
Shenzhen, Guangdong
Country
CHINAAddress
Ming Fai Industrial Estate, Bainikeng Pinghu, Longgang, Shenzhen, 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
DRUG GMPS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the methods used in and controls used for the manufacture, processing, packing, or holding of drugs and other products do not appear to conform to current good manufacturing practices within the meaning of Section 501(a)(2)(B).
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).
REGISTERED
It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).
FALSE
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose labeling appears to be false or misleading.
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.
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).
DE IMP GMP
The article is subject to refusal of admission pursuant to section 801(a)(1) in that it appears that the methods used in, or the facilities or controls used for, the manufacture of the device do not conform to the applicable requirements of section 520(f).
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.
SALMONELLA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/11/2024 | 76EFWTOOTHBRUSH, MANUAL | Division of Northern Border Imports (DNBI) | |
| 8/23/2024 | 62WBY99ASTRINGENT/ANTI-PERSPIRANT N.E.C. | 27DRUG GMPS | Division of Southeast Imports (DSEI) |
| 8/23/2024 | 53JD01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS) | 27DRUG GMPS | Division of Southeast Imports (DSEI) |
| 9/30/2019 | 53JY01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS) | 27DRUG GMPS | Division of Northeast Imports (DNEI) |
| 9/30/2019 | 53JY01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS) | 27DRUG GMPS | Division of Northeast Imports (DNEI) |
| 7/26/2018 | 61HAL99ANTI-BACTERIAL, N.E.C. | 27DRUG GMPS | Division of West Coast Imports (DWCI) |
| 4/4/2018 | 61HAL99ANTI-BACTERIAL, N.E.C. | 27DRUG GMPS | Division of West Coast Imports (DWCI) |
| 4/4/2018 | 61HAL99ANTI-BACTERIAL, N.E.C. | 27DRUG GMPS | Division of West Coast Imports (DWCI) |
| 4/4/2018 | 61HAL99ANTI-BACTERIAL, N.E.C. | 27DRUG GMPS | Division of West Coast Imports (DWCI) |
| 4/4/2018 | 61HAL99ANTI-BACTERIAL, N.E.C. | 27DRUG GMPS | Division of West Coast Imports (DWCI) |
| 3/30/2018 | 55QY41BENZALKONIUM CHLORIDE (PHARMACEUTIC NECESSITY - PRESERVATIVE) | 290DE IMP GMP | Division of West Coast Imports (DWCI) |
| 3/19/2018 | 61HAL99ANTI-BACTERIAL, N.E.C. | 27DRUG GMPS | Division of Northern Border Imports (DNBI) |
| 1/25/2018 | 63RAJ05SODIUM MONOFLUOROPHOSPHATE (DENTAL CARIES PROPHYLACTIC) | 27DRUG GMPS | Division of Northeast Imports (DNEI) |
| 9/6/2017 | 76JESFLOSS, DENTAL | Division of Northern Border Imports (DNBI) | |
| 1/14/2011 | 53IG01DENTIFRICES (AEROSOL, LIQUID, TOOTHPASTES, TOOTHPOWDERS), WITHOUT FLUORIDE (ORAL HYGIENE PRODUCTS) | 341REGISTERED | New York District Office (NYK-DO) |
| 11/20/2008 | 63RDY06STANNOUS FLUORIDE (DENTAL CARIES PROPHYLACTIC) | New York District Office (NYK-DO) | |
| 10/14/2008 | 76EFWTOOTHBRUSH, MANUAL | Los Angeles District Office (LOS-DO) | |
| 10/14/2008 | 53IG01DENTIFRICES (AEROSOL, LIQUID, TOOTHPASTES, TOOTHPOWDERS), WITHOUT FLUORIDE (ORAL HYGIENE PRODUCTS) | 9SALMONELLA | Los Angeles District Office (LOS-DO) |
| 10/31/2007 | 76NXZKIT, DENTAL HYGIENE | 310POISONOUS | Los Angeles District Office (LOS-DO) |
| 10/31/2007 | 53LD03FACE,BODY,AND HAND (EXCLUDING SHAVING PREPARATIONS) (SKIN CARE PREPARATIONS) | Los Angeles District Office (LOS-DO) | |
| 10/31/2007 | 53LD03FACE,BODY,AND HAND (EXCLUDING SHAVING PREPARATIONS) (SKIN CARE PREPARATIONS) | Los Angeles District Office (LOS-DO) | |
| 10/31/2007 | 53JF99OTHER PERSONAL CLEANLINESS PRODUCTS (NOT ANTIPERSPIRANT), N.E.C. | Los Angeles District Office (LOS-DO) | |
| 10/31/2007 | 53JF99OTHER PERSONAL CLEANLINESS PRODUCTS (NOT ANTIPERSPIRANT), N.E.C. | Los Angeles District Office (LOS-DO) | |
| 10/31/2007 | 62MAJ08MENTHOL (ANTI-PRURITIC) | 118NOT LISTED | Los Angeles District Office (LOS-DO) |
| 10/31/2007 | 53GI99OTHER MAKEUP PREPARATION, NOT FOR THE EYES, N.E.C. | 118NOT LISTED | Los Angeles District Office (LOS-DO) |
| 9/5/2007 | 76NXZKIT, DENTAL HYGIENE | Los Angeles District Office (LOS-DO) | |
| 3/27/2006 | 53BY01BATH OILS, TABLETS AND SALTS (BATH PREPARATIONS) | 471CSTIC LBLG | Cincinnati District Office (CIN-DO) |
Frequently Asked Questions
What is Ming Fai Industrial (Shenzhen) Co LTD's FDA import refusal history?
Ming Fai Industrial (Shenzhen) Co LTD (FEI: 3003340745) has 27 FDA import refusal record(s) in our database, spanning from 3/27/2006 to 9/11/2024.
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. Ming Fai Industrial (Shenzhen) Co LTD's FEI number is 3003340745.
What types of violations has Ming Fai Industrial (Shenzhen) Co LTD received?
Ming Fai Industrial (Shenzhen) Co LTD has been cited for 10 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 Ming Fai Industrial (Shenzhen) Co LTD come from?
All FDA import refusal data for Ming Fai Industrial (Shenzhen) 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.