FDA Inspection 1010391 — Tiina Karppa, M.D.

Tiina Karppa, M.D. — FEI 3013438176

The FDA completed an inspection of Tiina Karppa, M.D. on April 27, 2017 in Helsinki. 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
April 27, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Helsinki (Finland)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
753021 CFR 312.62(b)Case history records- inadequate or inadequate