FDA inspection

Videomed SRL: FDA inspection ending Mar 21, 2024

FDA inspection 1234785 · No Action Indicated (NAI) · Pordenone

Key facts

Inspection ID 1234785
Firm Videomed SRL
FEI number 3019252669
Address Interporto Centro Ingrosso 81
City Pordenone
Country Italy
Fiscal year 2024
Inspection end date Mar 21, 2024
Classification No Action Indicated (NAI)
Project area Compliance: 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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