FDA inspection

Shiono Finesse, Ltd.: FDA inspection ending Oct 24, 2025

FDA inspection 1292866 · No Action Indicated (NAI) · Sakai

Key facts

Inspection ID 1292866
Firm Shiono Finesse, Ltd.
FEI number 3005940219
Address 156-1 Aza-Hamawari, Yonozu 49, Mikunichoyonozu
City Sakai
Country Japan
Fiscal year 2026
Inspection end date Oct 24, 2025
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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