FDA inspection

OLYMPUS MEDICAL SYSTEMS CORP. Hinode Plant: FDA inspection ending Jul 29, 2010

FDA inspection 678583 · No Action Indicated (NAI) · Nishitama-Gun

Key facts

Inspection ID 678583
Firm OLYMPUS MEDICAL SYSTEMS CORP. Hinode Plant
FEI number 3003637092
Address 34-3, Oazahirai; Hinode-Machi
City Nishitama-Gun
Country Japan
Fiscal year 2010
Inspection end date Jul 29, 2010
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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