FDA inspection

Zeltiq Aesthetics, Inc: FDA inspection ending Mar 11, 2016

FDA inspection 980740 · No Action Indicated (NAI) · Pleasanton, CA

Key facts

Inspection ID 980740
Firm Zeltiq Aesthetics, Inc
FEI number 3007215625
Address 4410 Rosewood Dr
City Pleasanton
State CA
ZIP 94588
Country United States
Fiscal year 2016
Inspection end date Mar 11, 2016
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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