FDA Inspection 1191683 — 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 November 10, 2022 in Nishitama-Gun. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
November 10, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Nishitama-Gun (Japan)