FDA inspection

Sientra, Inc: FDA inspection ending Nov 16, 2012

FDA inspection 807414 · No Action Indicated (NAI) · Irvine, CA

Key facts

Inspection ID 807414
Firm Sientra, Inc
FEI number 3001628772
Address 3333 Michelson Dr Ste 650
City Irvine
State CA
ZIP 92612
Country United States
Fiscal year 2013
Inspection end date Nov 16, 2012
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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