FDA inspection

FUJIFILM Healthcare Americas Corporation: FDA inspection ending Dec 13, 2010

FDA inspection 706457 · Voluntary Action Indicated (VAI) · Wayne, NJ

Key facts

Inspection ID 706457
Firm FUJIFILM Healthcare Americas Corporation
FEI number 2431293
Address 10 Highpoint Dr
City Wayne
State NJ
ZIP 07470
Country United States
Fiscal year 2011
Inspection end date Dec 13, 2010
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

Browse all FDA inspections