FDA inspection

EEG Info: FDA inspection ending Mar 19, 2012

FDA inspection 772777 · Official Action Indicated (OAI) · Woodland Hills, CA

Key facts

Inspection ID 772777
Firm EEG Info
FEI number 3009138210
Address 6400 Canoga Ave Ste 210
City Woodland Hills
State CA
ZIP 91367
Country United States
Fiscal year 2012
Inspection end date Mar 19, 2012
Classification Official Action Indicated (OAI)
Project area Compliance: Devices
Product type Devices
Warning letter 296398

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • Yes 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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