FDA Inspection 794759 — OLYMPUS MEDICAL SYSTEMS CORP. Hinode Plant
The FDA completed an inspection of OLYMPUS MEDICAL SYSTEMS CORP. Hinode Plant on July 26, 2012 in Nishitama-Gun. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- July 26, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Nishitama-Gun (Japan)