FDA inspection

Ultroid Technologies, Inc.: FDA inspection ending Feb 12, 2014

FDA inspection 865741 · Voluntary Action Indicated (VAI) · Tampa, FL

Key facts

Inspection ID 865741
Firm Ultroid Technologies, Inc.
FEI number 3004892080
Address 103 W Main St
City Tampa
State FL
ZIP 33609
Country United States
Fiscal year 2014
Inspection end date Feb 12, 2014
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 10–99 Citations
  • 1–9 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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