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Nippon Kayaku Pharmatech Co., Ltd., Toyama, Japan – FDA Inspections

Inspection records and compliance data for Nippon Kayaku Pharmatech Co., Ltd. in Toyama. 2 FDA inspections on record, 1 Form 483, last inspected September 04, 2026.

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Company Profile

This profile covers Nippon Kayaku Pharmatech Co., Ltd. based in Toyama, Japan.

FDA Inspection History

FDA inspections
2
OAI
0
VAI
1
NAI
0
Unclassified
1
Form 483s
1
Warning letters
0

First inspected November 25, 2022. Last inspected September 4, 2026.

Most cited issue areas

  • Procedures for sterile drug products2 inspections
  • Active ingredient retained sample kept1 inspection
  • Calibration/Inspection/Checking not done1 inspection

FDA inspections (2)

DateResultFDA center(s)Insp. #
September 4, 2026Not classifiedHuman Drugs · Drug Quality Assurance1335048
November 25, 2022VAIHuman Drugs · Drug Quality Assurance1192063
FDA documents

Form 483s (4)

  • Form 483s · September 4, 2026
  • Form 483s · November 25, 2022
  • Form 483s · November 25, 2020
  • Form 483s · November 26, 2019
People (3)
Darren S. Brown
Person
Robert Scott
Person
Robert J. Martin
Person
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Company Information

Name

Nippon Kayaku Pharmatech Co., Ltd.

FEI Number

3008538640

Address

750,, Fuchumachiitakura, Toyama, Japan

Country

Japan

ID: 88530942-e172-4a65-8c32-4495fdaa6b61

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