FDA inspection

SUZUKEN CO., LTD. OGUCHI CENTER: FDA inspection ending Dec 15, 2010

FDA inspection 708074 · Voluntary Action Indicated (VAI) · Niwa-Gun

Key facts

Inspection ID 708074
Firm SUZUKEN CO., LTD. OGUCHI CENTER
FEI number 3006540105
Address 1 Chome 58-1, Totsubo; Oguchi-Cho
City Niwa-Gun
Country Japan
Fiscal year 2011
Inspection end date Dec 15, 2010
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes 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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