ImportRefusal LogoImportRefusal

Kitazato Corporation

⚠️ Moderate Risk

FEI: 3008876063 • Fuji, Shizuoka • JAPAN

FEI

FEI Number

3008876063

📍

Location

Fuji, Shizuoka

🇯🇵

Country

JAPAN
🏢

Address

100-10, Yanagishima, Fuji, Shizuoka, Japan

Moderate Risk

FDA Import Risk Assessment

45.2
LowModerateHighCritical

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

Statistics

15
Total Refusals
3
Unique Violations
6/7/2012
Latest Refusal
8/5/2011
Earliest Refusal

Score Breakdown

Violation Severity
54.6×40%
Refusal Volume
44.6×30%
Recency
0.0×20%
Frequency
100.0×10%
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

11814×

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).

5089×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

3413×

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).

Refusal History

DateProductViolationsDivision
6/7/2012
75LXGEQUIPMENT, LABORATORY, GENERAL PURPOSE, LABELED OR PROMOTED FOR A SPECIFIC MEDICAL USE
118NOT LISTED
New Orleans District Office (NOL-DO)
6/7/2012
75LXGEQUIPMENT, LABORATORY, GENERAL PURPOSE, LABELED OR PROMOTED FOR A SPECIFIC MEDICAL USE
118NOT LISTED
New Orleans District Office (NOL-DO)
3/20/2012
85MQENEEDLE, ASSISTED REPRODUCTION
118NOT LISTED
508NO 510(K)
New Orleans District Office (NOL-DO)
3/2/2012
85MQLMEDIA, REPRODUCTIVE
118NOT LISTED
341REGISTERED
508NO 510(K)
New Orleans District Office (NOL-DO)
3/2/2012
85MQLMEDIA, REPRODUCTIVE
118NOT LISTED
341REGISTERED
508NO 510(K)
New Orleans District Office (NOL-DO)
1/7/2012
85MQLMEDIA, REPRODUCTIVE
118NOT LISTED
New Orleans District Office (NOL-DO)
1/6/2012
85MQHMICROTOOLS, ASSISTED REPRODUCTION (PIPETTES)
341REGISTERED
New Orleans District Office (NOL-DO)
12/20/2011
85MQHMICROTOOLS, ASSISTED REPRODUCTION (PIPETTES)
118NOT LISTED
508NO 510(K)
New Orleans District Office (NOL-DO)
10/12/2011
85MQHMICROTOOLS, ASSISTED REPRODUCTION (PIPETTES)
118NOT LISTED
508NO 510(K)
New Orleans District Office (NOL-DO)
10/12/2011
85MQHMICROTOOLS, ASSISTED REPRODUCTION (PIPETTES)
118NOT LISTED
508NO 510(K)
New Orleans District Office (NOL-DO)
10/12/2011
85MQHMICROTOOLS, ASSISTED REPRODUCTION (PIPETTES)
118NOT LISTED
508NO 510(K)
New Orleans District Office (NOL-DO)
9/9/2011
85MQLMEDIA, REPRODUCTIVE
118NOT LISTED
New Orleans District Office (NOL-DO)
8/23/2011
85MQKLABWARE, ASSISTED REPRODUCTION
118NOT LISTED
508NO 510(K)
New Orleans District Office (NOL-DO)
8/23/2011
85MQLMEDIA, REPRODUCTIVE
118NOT LISTED
508NO 510(K)
New Orleans District Office (NOL-DO)
8/5/2011
85MQLMEDIA, REPRODUCTIVE
118NOT LISTED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Kitazato Corporation's FDA import refusal history?

Kitazato Corporation (FEI: 3008876063) has 15 FDA import refusal record(s) in our database, spanning from 8/5/2011 to 6/7/2012.

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. Kitazato Corporation's FEI number is 3008876063.

What types of violations has Kitazato Corporation received?

Kitazato Corporation has been cited for 3 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 Kitazato Corporation come from?

All FDA import refusal data for Kitazato Corporation 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.