FDA Inspection
Howard M. Richard, III M.D.Howard M. Richard, III M.D. – FDA Inspection, Mar 6, 2023
Record Details
This FDA Inspection record concerns Howard M. Richard, III M.D., with an inspection on March 6, 2023, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 7c3a1b3a-c9de-46df-90e9-9f14f4200584
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1199068
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
- Outcome
- Form 483 issued
FDA Citations
4- 21 CFR 812.100Investigator non-compliance with agreement/plan/regulations
- 21 CFR 812.140(a)(2)(i)Investigator device accountability inadequate
- 21 CFR 812.100Investigator non-compliance with agreement/plan/regulations
- 21 CFR 812.140(a)(2)(i)Investigator device accountability inadequate
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