FDA Inspection
Castellvi Antonio, MDCastellvi Antonio, MD – FDA Inspection, Mar 18, 2009
Record Details
This FDA Inspection record concerns Castellvi Antonio, MD, with an inspection on March 18, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Castellvi Antonio, MD
- Inspection Date
- March 18, 2009
- Product Type
- Devices
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ID · 8e3f2ab2-dfea-4fe0-8512-d4cea9e9e5f1
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 571650
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
3- 21 CFR 812.140(a)(3)(i)Investigator records of informed consent inadequate
- 21 CFR 812.140(a)(3)(ii)Investigator adverse effect records inadequate
- 21 CFR 812.140(a)(3)Investigator"s subject records inadequate
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Other FDA inspections of Castellvi Antonio, MD
1| Date | Classification | Office | Project area |
|---|---|---|---|
| March 21, 2012 | VAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Castellvi Antonio, MD
- FDA Inspection 773793 - 2012-03-21
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