FDA Inspection
Brett C Meyer MdBrett C Meyer Md – FDA Inspection, Jul 30, 2010
Record Details
This FDA Inspection record concerns Brett C Meyer Md, with an inspection on July 30, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Brett C Meyer Md
- Inspection Date
- July 30, 2010
- Product Type
- Devices
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ID · 2a4b002b-3902-4080-a2f9-f70ef41948a4
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 675157
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
2- 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
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