FDA Inspection
Posy Seifert, DOPosy Seifert, DO – FDA Inspection, Apr 3, 2014
Record Details
This FDA Inspection record concerns Posy Seifert, DO, with an inspection on April 3, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Posy Seifert, DO
- Inspection Date
- April 3, 2014
- Product Type
- Devices
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ID · 171e6b17-dee2-4b4e-b1cd-664fb3f3e9c2
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 875071
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
3- 21 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations
- 21 CFR 812.140(a)(3)(i)Investigator records of informed consent inadequate
- 21 CFR 812.110(d)Inadequate financial disclosure by investigator
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