FDA inspection

Invivo Corporation: FDA inspection ending Aug 17, 2015

FDA inspection 938698 · Voluntary Action Indicated (VAI) · Orlando, FL

Key facts

Inspection ID 938698
Firm Invivo Corporation
FEI number 1051786
Address 12151 Research Pkwy Ste 200
City Orlando
State FL
ZIP 32826
Country United States
Fiscal year 2015
Inspection end date Aug 17, 2015
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 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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