FDA Inspection
Philips Medizin Systeme Boeblingen GmbhPhilips Medizin Systeme Boeblingen Gmbh – FDA Inspection, Jan 29, 2015
Record Details
This FDA Inspection record concerns Philips Medizin Systeme Boeblingen Gmbh, with an inspection on January 29, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- January 29, 2015
- Product Type
- Devices
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ID · 5778c169-80e8-4d9c-ae96-08e394a2fa34
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 913852
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 803.50(a)(2)Individual Report of Malfunction
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