FDA inspection

Trinity Medical Devices, Inc.: FDA inspection ending May 7, 2025

FDA inspection 1269741 · Voluntary Action Indicated (VAI) · Morristown, NJ

Key facts

Inspection ID 1269741
Firm Trinity Medical Devices, Inc.
FEI number 3010042047
Address 43 Speedwell Ave # 1251
City Morristown
State NJ
ZIP 07960
Country United States
Fiscal year 2025
Inspection end date May 7, 2025
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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