FDA Inspection 800481 — Marek B. Kunecki, M.D.

Marek B. Kunecki, M.D. — FEI 3009466547

The FDA completed an inspection of Marek B. Kunecki, M.D. on Aug 30, 2012 in Lodz. 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). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 30, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Lodz (Poland)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
756021 CFR 312.60FD-1572, protocol compliance