FDA Inspection 1250006 — Sony Global Manufacturing & Operations Corporation-Kohda Site

Sony Global Manufacturing & Operations Corporation-Kohda Site — FEI 3016527960

The FDA completed an inspection of Sony Global Manufacturing & Operations Corporation-Kohda Site on Jul 26, 2024 in Nukata-Gun. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 26, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Nukata-Gun (Japan)