FDA Inspection
Ruth E. Tedaldi, MDRuth E. Tedaldi, MD – FDA Inspection, Aug 25, 2014
Record Details
This FDA Inspection record concerns Ruth E. Tedaldi, MD, with an inspection on August 25, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Ruth E. Tedaldi, MD
- Inspection Date
- August 25, 2014
- Product Type
- Devices
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ID · 945d7069-08cc-4216-8466-09a49256a2df
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 892732
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
1- 21 CFR 812.140(a)(3)Investigator"s subject records inadequate
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