# Philips Respironics, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/philips-respironics-inc/03ceee46-7a72-4590-8bc4-8033e1503cf3

> Inspection records and compliance data for Philips Respironics, Inc. in Murrysville, Pennsylvania. Access full analysis and detailed observations.

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## Details

- Name: Philips Respironics, Inc.
- FEI Number: 2518422
- City: Murrysville
- State: Pennsylvania
- Country Name: United States
- Address Line 1: 1001 Murry Ridge Ln
- Zip Code: 15668
- Facility Type: Medical Device Manufacturer

## Related Documents

- [FDA Inspection 1170199 - Philips Respironics, Inc. - 2022-05-19](https://www.keypedia.com/records/fda_inspections/philips-respironics-inc/7dcc20c7-b932-4d4c-a2a3-4fd41f0c072d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 19, 2022
- [FDA Inspection 1170199 - Philips Respironics, Inc. - 2022-05-19](https://www.keypedia.com/records/fda_inspections/philips-respironics-inc/a340b016-c264-4077-a9f9-78eaedb39a99) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 19, 2022
- [483 - Philips Respironics, Inc. - 2021-11-09](https://www.keypedia.com/records/483/philips-respironics-inc/45c9eb4c-757c-47bf-97da-f808aab5c64b) — source: FDA, date: November 9, 2021
- [483 - Philips Respironics, Inc. - 2021-11-09](https://www.keypedia.com/records/483/philips-respironics-inc/dd37d2e1-0043-4f9e-bf2a-68de84a73aef) — source: FDA, date: November 9, 2021
- [FDA Inspection 1156266 - Philips Respironics, Inc. - 2021-11-09](https://www.keypedia.com/records/fda_inspections/philips-respironics-inc/85f9615e-35ee-4db7-ac1b-820ea4c67f7d) — classification: Official Action Indicated (OAI), source: FDA, date: November 9, 2021
- [FDA Inspection 1156266 - Philips Respironics, Inc. - 2021-11-09](https://www.keypedia.com/records/fda_inspections/philips-respironics-inc/e7e4ddcf-5990-4fee-b9cb-45ce1e064695) — classification: Official Action Indicated (OAI), source: FDA, date: November 9, 2021
- [FDA Inspection 1151497 - Philips Respironics, Inc. - 2021-09-10](https://www.keypedia.com/records/fda_inspections/philips-respironics-inc/b4840ec4-15e1-4721-b67d-65c99aae89c6) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 10, 2021
- [FDA Inspection 1114919 - Philips Respironics, Inc. - 2020-01-10](https://www.keypedia.com/records/fda_inspections/philips-respironics-inc/e3437ea2-fa89-4638-923a-9d9e4b6648f6) — classification: Official Action Indicated (OAI), source: FDA, date: January 10, 2020
- [FDA Inspection 1056962 - Philips Respironics, Inc. - 2018-05-21](https://www.keypedia.com/records/fda_inspections/philips-respironics-inc/56b347f0-3856-440c-a7b6-94ead1e86b9b) — classification: Official Action Indicated (OAI), source: FDA, date: May 21, 2018
- [FDA Inspection 1056962 - Philips Respironics, Inc. - 2018-05-21](https://www.keypedia.com/records/fda_inspections/philips-respironics-inc/1a35ebca-0bb1-4b5f-9d2a-407db3afbeda) — classification: Official Action Indicated (OAI), source: FDA, date: May 21, 2018
- [FDA Inspection 954800 - Philips Respironics, Inc. - 2016-01-15](https://www.keypedia.com/records/fda_inspections/philips-respironics-inc/6bf53a57-0b7d-4458-bce6-46a6e267e61a) — classification: Official Action Indicated (OAI), source: FDA, date: January 15, 2016
- [FDA Inspection 954800 - Philips Respironics, Inc. - 2016-01-15](https://www.keypedia.com/records/fda_inspections/philips-respironics-inc/d26edac4-065d-4423-a95e-f3b3a5097fcd) — classification: Official Action Indicated (OAI), source: FDA, date: January 15, 2016

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