FDA inspection

Philips Respironics, Inc.: FDA inspection ending Jan 10, 2020

FDA inspection 1114919 · Official Action Indicated (OAI) · Murrysville, PA

Key facts

Inspection ID 1114919
Firm Philips Respironics, Inc.
FEI number 2518422
Address 2271 Cosmos Ct
City Murrysville
State PA
ZIP 15668
Country United States
Fiscal year 2020
Inspection end date Jan 10, 2020
Classification Official Action Indicated (OAI)
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
  • 10–99 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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