FDA inspection

Sony Global Manufacturing & Operations Corporation-Kohda Site: FDA inspection ending Jul 26, 2024

FDA inspection 1250006 · Voluntary Action Indicated (VAI) · Nukata-Gun

Key facts

Inspection ID 1250006
Firm Sony Global Manufacturing & Operations Corporation-Kohda Site
FEI number 3016527960
Address Soniiemushiesu (Kabu) Kodatekku, Azasuzumegairi; Oazasakazaki; Kota-Cho
City Nukata-Gun
Country Japan
Fiscal year 2024
Inspection end date Jul 26, 2024
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

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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