FDA inspection

Philips Respironics, Inc.: FDA inspection ending Sep 3, 2014

FDA inspection 895553 · No Action Indicated (NAI) · Murrysville, PA

Key facts

Inspection ID 895553
Firm Philips Respironics, Inc.
FEI number 2518422
Address 2271 Cosmos Ct
City Murrysville
State PA
ZIP 15668
Country United States
Fiscal year 2014
Inspection end date Sep 3, 2014
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
  • 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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