FDA Inspection
Kirk Reichard, MDKirk Reichard, MD – FDA Inspection, Mar 1, 2011
Record Details
This FDA Inspection record concerns Kirk Reichard, MD, with an inspection on March 1, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Kirk Reichard, MD
- Inspection Date
- March 1, 2011
- Product Type
- Devices
View Company Profile
ID · 88f3d3cd-2817-4c00-b713-98bd1842445f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 711791
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
6- 21 CFR 812.150(a)(1)Investigator report of unanticipated adverse effects
- 21 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations
- 21 CFR 812.140(a)(3)(ii)Investigator records of relevant observations inadequate
- 21 CFR 812.140(a)(3)Investigator"s subject records inadequate
- 21 CFR 812.140(a)(2)(i)Investigator device accountability inadequate
- 21 CFR 812.140(a)(4)Investigator record of protocol deviations inadequate
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