FDA Inspection 678583 — OLYMPUS MEDICAL SYSTEMS CORP. Hinode Plant

OLYMPUS MEDICAL SYSTEMS CORP. Hinode Plant — FEI 3003637092

The FDA completed an inspection of OLYMPUS MEDICAL SYSTEMS CORP. Hinode Plant on July 29, 2010 in Nishitama-Gun. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 29, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Nishitama-Gun (Japan)