FDA Inspection
Comm Gen Hospital Investigative & New Procedures CommitteeComm Gen Hospital Investigative & New Procedures Committee – FDA Inspection, Nov 3, 2009
Record Details
This FDA Inspection record concerns Comm Gen Hospital Investigative & New Procedures Committee, with an inspection on November 3, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- November 3, 2009
- Product Type
- Devices
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ID · bf415ba3-240d-487e-82d5-f588eb8c373e
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 629826
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
5- 21 CFR 56.115(a)(5)List of members
- 21 CFR 56.115(a)(2)Minutes of IRB meetings
- 21 CFR 56.108(a)(1)Initial and continuing reviews
- 21 CFR 56.110(b)(2)Minor changes
- 21 CFR 56.110(c)Method to keep members advised
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