FDA inspection

AdventHealth Orlando - IRB: FDA inspection ending Jul 30, 2015

FDA inspection 936680 · No Action Indicated (NAI) · Orlando, FL

Key facts

Inspection ID 936680
Firm AdventHealth Orlando - IRB
FEI number 1036720
Address 901 N Lake Destiny Rd
City Orlando
State FL
ZIP 32803
Country United States
Fiscal year 2015
Inspection end date Jul 30, 2015
Classification No Action Indicated (NAI)
Project area Bioresearch Monitoring
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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