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 Nov 10, 2022 in Nishitama-Gun. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.

Inspection Details

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

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