FDA Inspection 595025 — Heath, Karen

Heath, Karen — FEI 3007680724

The FDA completed an inspection of Heath, Karen on May 20, 2009 in San Carlos, AZ. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
May 20, 2009
Fiscal Year
2009
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
San Carlos, AZ (United States)

Additional Details

Clinical Investigator (CI)