FDA inspection

Cerus Corporation: FDA inspection ending Dec 15, 2015

FDA inspection 959787 · Voluntary Action Indicated (VAI) · Concord, CA

Key facts

Inspection ID 959787
Firm Cerus Corporation
FEI number 3003925919
Address 2550 Stanwell Dr
City Concord
State CA
ZIP 94520
Country United States
Fiscal year 2016
Inspection end date Dec 15, 2015
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
  • Yes 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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