FDA inspection

Silex Medical, LLC: FDA inspection ending Apr 23, 2025

FDA inspection 1268198 · Voluntary Action Indicated (VAI) · Southington, CT

Key facts

Inspection ID 1268198
Firm Silex Medical, LLC
FEI number 3005110411
Address 24 Robert Porter Rd Ste B
City Southington
State CT
ZIP 06489
Country United States
Fiscal year 2025
Inspection end date Apr 23, 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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