FDA Inspection
Philips Medizin Systeme Boeblingen GmbhPhilips Medizin Systeme Boeblingen Gmbh – FDA Inspection, Mar 7, 2024
Record Details
This FDA Inspection record concerns Philips Medizin Systeme Boeblingen Gmbh, with an inspection on March 7, 2024, issued by the Center for Devices and Radiological Health, covering devices.
View Company Profile
ID · 0ed3fffa-5269-411d-9d9e-a188339ef61e
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 1230548
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Philips Medizin Systeme Boeblingen Gmbh
4| Date | Classification | Office | Project area |
|---|---|---|---|
| November 24, 2017 | Not classified | Office of Inspections and Investigations | |
| January 29, 2015 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 14, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 23, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Philips Medizin Systeme Boeblingen Gmbh
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.