FDA Inspection 587806 — Krook, Dr. James E

Krook, Dr. James E — FEI 2127735

The FDA completed an inspection of Krook, Dr. James E on May 22, 2009 in Duluth, MN. 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: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
May 22, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Duluth, MN (United States)

Additional Details

Clinical Investigator (CI)