FDA inspection

TOKUYAMA SEKISUI CO., LTD.: FDA inspection ending Feb 1, 2017

FDA inspection 1001154 · Voluntary Action Indicated (VAI) · Shunan

Key facts

Inspection ID 1001154
Firm TOKUYAMA SEKISUI CO., LTD.
FEI number 3006850222
Address 4560, Kaisei-Machi
City Shunan
Country Japan
Fiscal year 2017
Inspection end date Feb 1, 2017
Classification Voluntary Action Indicated (VAI)
Project area Compliance: 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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