FDA inspection

AcuFocus, Inc.: FDA inspection ending Jan 18, 2013

FDA inspection 815296 · Voluntary Action Indicated (VAI) · Irvine, CA

Key facts

Inspection ID 815296
Firm AcuFocus, Inc.
FEI number 3008401069
Address 32 Discovery Ste 200
City Irvine
State CA
ZIP 92618
Country United States
Fiscal year 2013
Inspection end date Jan 18, 2013
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: Devices
Product type Devices

At a glance

  • None 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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