FDA Inspection
Philips BurtonPhilips Burton – FDA Inspection, Nov 10, 2011
Record Details
This FDA Inspection record concerns Philips Burton, with an inspection on November 10, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Philips Burton
- Inspection Date
- November 10, 2011
- Product Type
- Devices
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ID · 7faa4923-0467-4d63-8848-f246b6973c66
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 753037
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.100(b)Documentation
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