FDA inspection

Yuki Gosei Kogyo Co., Ltd.: FDA inspection ending Jul 28, 2021

FDA inspection 1149608 · Voluntary Action Indicated (VAI) · Iwaki

Key facts

Inspection ID 1149608
Firm Yuki Gosei Kogyo Co., Ltd.
FEI number 3002808534
Address Ochiai, Jobannishigo-Machi
City Iwaki
Country Japan
Fiscal year 2021
Inspection end date Jul 28, 2021
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes 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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