FDA inspection

Rapid Oxygen Inc.: FDA inspection ending Apr 26, 2024

FDA inspection 1230546 · Voluntary Action Indicated (VAI) · Shelton, CT

Key facts

Inspection ID 1230546
Firm Rapid Oxygen Inc.
FEI number 3014408327
Address 88 Long Hill Cross Rd
City Shelton
State CT
ZIP 06484
Country United States
Fiscal year 2024
Inspection end date Apr 26, 2024
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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