FDA Inspection
Philips Medizin Systeme Boeblingen GmbhPhilips Medizin Systeme Boeblingen Gmbh – FDA Inspection, Jun 14, 2012
Record Details
This FDA Inspection record concerns Philips Medizin Systeme Boeblingen Gmbh, with an inspection on June 14, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- June 14, 2012
- Product Type
- Devices
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ID · fc835aa7-f441-4fe8-a965-866559918623
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 791970
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.120(d)Records, DHR {see also 820.184(e)}
- 21 CFR 803.17Lack of Written MDR Procedures
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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 |
| November 24, 2017 | Not classified | Office of Inspections and Investigations | |
| January 29, 2015 | 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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