FDA Inspection 918243 — Michael P. Whyte, MD

Michael P. Whyte, MD — FEI 3011343841

The FDA completed an inspection of Michael P. Whyte, MD on Mar 11, 2015 in Saint Louis, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 11, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Saint Louis, MO (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
752721 CFR 312.62(a)Unused drug disposition (investigator)
756021 CFR 312.60FD-1572, protocol compliance