FDA Inspection
Timothy Murphy, M.D.Timothy Murphy, M.D. – FDA Inspection, Mar 22, 2011
Record Details
This FDA Inspection record concerns Timothy Murphy, M.D., with an inspection on March 22, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Timothy Murphy, M.D.
- Inspection Date
- March 22, 2011
- Product Type
- Devices
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ID · a4c7ad9b-69ec-4851-9995-ebfc36cfef56
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 719170
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
2- 21 CFR 812.43(c)No investigator agreement
- 21 CFR 812.140(b)(1)Sponsor correspondence records inadequate
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