FDA inspection

DuoProSS Meditech Corporation: FDA inspection ending May 22, 2025

FDA inspection 1275558 · No Action Indicated (NAI) · Farmingdale, NY

Key facts

Inspection ID 1275558
Firm DuoProSS Meditech Corporation
FEI number 3003681915
Address 154 Marine St
City Farmingdale
State NY
ZIP 11735
Country United States
Fiscal year 2025
Inspection end date May 22, 2025
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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