FDA Inspection 932673 — Alan P. Knutsen, M.D.

Alan P. Knutsen, M.D. — FEI 3011562221

The FDA completed an inspection of Alan P. Knutsen, M.D. on June 29, 2015 in Saint Louis, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 29, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Saint Louis, MO (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
756021 CFR 312.60FD-1572, protocol compliance