FDA Inspection 568341 — Kevin L. Russell

Kevin L. Russell — FEI 3007444374

The FDA completed an inspection of Kevin L. Russell on Mar 13, 2009 in Frederick, MD. 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). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 13, 2009
Fiscal Year
2009
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Frederick, MD (United States)

Additional Details

Clinical Investigator (CI)