FDA Inspection 751463 — SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION

SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION — FEI 3002808139

The FDA completed an inspection of SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION on Sep 9, 2011 in Kyoto. 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
Sep 9, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Kyoto (Japan)

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