FDA inspection

Prexion, Inc.: FDA inspection ending Dec 26, 2013

FDA inspection 858562 · Voluntary Action Indicated (VAI) · San Jose, CA

Key facts

Inspection ID 858562
Firm Prexion, Inc.
FEI number 3007038334
Address 2077 Gateway Pl Ste 120
City San Jose
State CA
ZIP 95110
Country United States
Fiscal year 2014
Inspection end date Dec 26, 2013
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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