FDA inspection

Universal Orlando Resort: FDA inspection ending May 1, 2018

FDA inspection 1060866 · No Action Indicated (NAI) · Orlando, FL

Key facts

Inspection ID 1060866
Firm Universal Orlando Resort
FEI number 1052415
Address 1000 Universal Studios Plz
City Orlando
State FL
ZIP 32819
Country United States
Fiscal year 2018
Inspection end date May 1, 2018
Classification No Action Indicated (NAI)
Project area Radiation Control and Health Safety Act
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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