FDA Inspection 998284 — Peter O'Donnell

Peter O'Donnell — FEI 3012922072

The FDA completed an inspection of Peter O'Donnell on January 19, 2017 in Chicago, IL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 4 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 19, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Chicago, IL (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
751821 CFR 312.64(d)Financial info
752021 CFR 312.64(b)Safety reports
753021 CFR 312.62(b)Case history records- inadequate or inadequate
756021 CFR 312.60FD-1572, protocol compliance