FDA inspection

Universal Orlando Resort: FDA inspection ending Feb 12, 2006

FDA inspection 412820 · No Action Indicated (NAI) · Orlando, FL

Key facts

Inspection ID 412820
Firm Universal Orlando Resort
FEI number 1052415
Address 1000 Universal Studios Plz
City Orlando
State FL
ZIP 32819-7601
Fiscal year 2006
Inspection end date Feb 12, 2006
Classification No Action Indicated (NAI)
Project area Rad Cntrl & Hlth Safety Act (RCHSA) Auth
Product type Devices

At a glance

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