FDA Inspection 843960 — SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION
The FDA completed an inspection of SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION on Aug 1, 2013 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
- Aug 1, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Kyoto (Japan)