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Ming Fai Industrial (Shenzhen) Co LTD

⚠️ High Risk

FEI: 3003340745 • Shenzhen, Guangdong • CHINA

FEI

FEI Number

3003340745

📍

Location

Shenzhen, Guangdong

🇨🇳

Country

CHINA
🏢

Address

Ming Fai Industrial Estate, Bainikeng Pinghu, Longgang, Shenzhen, Guangdong, China

High Risk

FDA Import Risk Assessment

57.2
LowModerateHighCritical

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

Statistics

27
Total Refusals
10
Unique Violations
9/11/2024
Latest Refusal
3/27/2006
Earliest Refusal

Score Breakdown

Violation Severity
62.7×40%
Refusal Volume
53.6×30%
Recency
73.0×20%
Frequency
14.6×10%
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

2711×

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).

1189×

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).

3415×

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).

2234×

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.

32802×

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.

752×

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).

2901×

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).

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.

91×

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.

3101×

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

DateProductViolationsDivision
9/11/2024
76EFWTOOTHBRUSH, MANUAL
3280FRNMFGREG
341REGISTERED
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
118NOT LISTED
3280FRNMFGREG
341REGISTERED
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)
118NOT LISTED
75UNAPPROVED
New York District Office (NYK-DO)
10/14/2008
76EFWTOOTHBRUSH, MANUAL
118NOT LISTED
341REGISTERED
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)
118NOT LISTED
223FALSE
Los Angeles District Office (LOS-DO)
10/31/2007
53LD03FACE,BODY,AND HAND (EXCLUDING SHAVING PREPARATIONS) (SKIN CARE PREPARATIONS)
118NOT LISTED
223FALSE
Los Angeles District Office (LOS-DO)
10/31/2007
53JF99OTHER PERSONAL CLEANLINESS PRODUCTS (NOT ANTIPERSPIRANT), N.E.C.
118NOT LISTED
223FALSE
Los Angeles District Office (LOS-DO)
10/31/2007
53JF99OTHER PERSONAL CLEANLINESS PRODUCTS (NOT ANTIPERSPIRANT), N.E.C.
118NOT LISTED
223FALSE
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
341REGISTERED
75UNAPPROVED
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.