FDA Inspection 925052 — Kitazato Corporation

Kitazato Corporation — FEI 3008876063

The FDA completed an inspection of Kitazato Corporation on Apr 16, 2015 in Fuji. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Apr 16, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Fuji (Japan)

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