FDA Inspection
Philips Medizin Systeme Boeblingen GmbhPhilips Medizin Systeme Boeblingen Gmbh – FDA Inspection, Nov 24, 2017
Record Details
This FDA Inspection record concerns Philips Medizin Systeme Boeblingen Gmbh, with an inspection on November 24, 2017, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Inspection Date
- November 24, 2017
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · c9d03162-9df8-4273-ad28-8f095c275d94
Inspection Facts
- Inspection number
- 1050977
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Philips Medizin Systeme Boeblingen Gmbh
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|---|---|---|---|
| March 7, 2024 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| 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 |
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