FDA inspection

Vivorte, Inc.: FDA inspection ending Nov 23, 2021

FDA inspection 1157349 · Voluntary Action Indicated (VAI) · Louisville, KY

Key facts

Inspection ID 1157349
Firm Vivorte, Inc.
FEI number 3010642815
Address 1044 E Chestnut St
City Louisville
State KY
ZIP 40204
Country United States
Fiscal year 2022
Inspection end date Nov 23, 2021
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
  • 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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