FDA inspection

Shiono Finesse, Ltd.: FDA inspection ending Nov 7, 2014

FDA inspection 907474 · Voluntary Action Indicated (VAI) · Sakai

Key facts

Inspection ID 907474
Firm Shiono Finesse, Ltd.
FEI number 3005940219
Address 156-1 Aza-Hamawari, Yonozu 49, Mikunichoyonozu
City Sakai
Country Japan
Fiscal year 2015
Inspection end date Nov 7, 2014
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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