FDA Inspection 826373 — Nikkiso Ltd - Shizuoka Plant

Nikkiso Ltd - Shizuoka Plant — FEI 3002807721

The FDA completed an inspection of Nikkiso Ltd - Shizuoka Plant on Mar 7, 2013 in Makinohara. 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
Mar 7, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Makinohara (Japan)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.