FDA inspection

Philips Respironics, Inc.: FDA inspection ending Dec 5, 2013

FDA inspection 858599 · No Action Indicated (NAI) · Murrysville, PA

Key facts

Inspection ID 858599
Firm Philips Respironics, Inc.
FEI number 2518422
Address 1001 Murry Ridge Ln
City Murrysville
State PA
ZIP 15668
Country United States
Fiscal year 2014
Inspection end date Dec 5, 2013
Classification No Action Indicated (NAI)
Project area Postmarket Assurance: 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
  • 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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