FDA inspection

Sankyo Kasei Co., Ltd.: FDA inspection ending Jan 31, 2020

FDA inspection 1118502 · No Action Indicated (NAI) · Fukuchiyama

Key facts

Inspection ID 1118502
Firm Sankyo Kasei Co., Ltd.
FEI number 3008342971
Address 1 Chome 58-1 Plant No.2, Osadano-Cho
City Fukuchiyama
Country Japan
Fiscal year 2020
Inspection end date Jan 31, 2020
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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