FDA inspection

Unisis Corp.: FDA inspection ending Feb 19, 2016

FDA inspection 959727 · No Action Indicated (NAI) · Koshigaya

Key facts

Inspection ID 959727
Firm Unisis Corp.
FEI number 3003803331
Address Koshigaya City, Saitama, 2675-1; Nishikata
City Koshigaya
Country Japan
Fiscal year 2016
Inspection end date Feb 19, 2016
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

Browse all FDA inspections