FDA Inspection 910840 — Michael P. Husseman, MD

Michael P. Husseman, MD — FEI 3005337671

The FDA completed an inspection of Michael P. Husseman, MD on Dec 23, 2014 in Layton, UT. 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: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 23, 2014
Fiscal Year
2015
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Layton, UT (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
753021 CFR 312.62(b)Case history records- inadequate or inadequate
756021 CFR 312.60FD-1572, protocol compliance