FDA Inspection 896542 — Derek D. Muse, M.D., Clinical Investigator

Derek D. Muse, M.D., Clinical Investigator — FEI 3010873299

The FDA completed an inspection of Derek D. Muse, M.D., Clinical Investigator on July 18, 2014 in Salt Lake City, UT. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 18, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Salt Lake City, UT (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
736321 CFR 50.55(f)Documentation of permission by parents or guardian
753021 CFR 312.62(b)Case history records- inadequate or inadequate
756021 CFR 312.60FD-1572, protocol compliance