FDA Inspection
Peter Helton M.D.Peter Helton M.D. – FDA Inspection, Jul 12, 2013
Record Details
This FDA Inspection record concerns Peter Helton M.D., with an inspection on July 12, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Peter Helton M.D.
- Inspection Date
- July 12, 2013
- Product Type
- Devices
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ID · b9670826-cc7e-4694-8e3c-5f10be6cf35c
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 840881
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
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