FDA inspection

Candelis Inc: FDA inspection ending Dec 16, 2011

FDA inspection 793994 · Newport Beach, CA

Key facts

Inspection ID 793994
Firm Candelis Inc
FEI number 3005919188
Address 4701 Von Karman Ave Ste 200
City Newport Beach
State CA
ZIP 92660-2192
Fiscal year 2012
Inspection end date Dec 16, 2011
Product type Devices

At a glance

  • None Citations
  • None 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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