FDA Inspection
Janet Bay MDJanet Bay MD – FDA Inspection, Mar 31, 2009
Record Details
This FDA Inspection record concerns Janet Bay MD, with an inspection on March 31, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Janet Bay MD
- Inspection Date
- March 31, 2009
- Product Type
- Devices
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ID · b00395af-d27c-4083-bd81-2ee36cded947
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 568581
- 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 812.150(a)(3)No investigator progress reports
- 21 CFR 812.140(a)(3)Investigator"s subject records inadequate
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