FDA inspection

Apixia Inc: FDA inspection ending Jun 11, 2015

FDA inspection 932609 · No Action Indicated (NAI) · City Of Industry, CA

Key facts

Inspection ID 932609
Firm Apixia Inc
FEI number 3008361230
Address 18688 San Jose Ave Ste 2
City City Of Industry
State CA
ZIP 91748
Country United States
Fiscal year 2015
Inspection end date Jun 11, 2015
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

Browse all FDA inspections