FDA Inspection 928672 — Agnieszka Jagiello-Gruszfeld, M.D., Mazurskim Centrum

Agnieszka Jagiello-Gruszfeld, M.D., Mazurskim Centrum — FEI 3005929862

The FDA completed an inspection of Agnieszka Jagiello-Gruszfeld, M.D., Mazurskim Centrum on Mar 20, 2015 in Olsztyn. 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). 2 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 20, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Olsztyn (Poland)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
753021 CFR 312.62(b)Case history records- inadequate or inadequate
756021 CFR 312.60FD-1572, protocol compliance

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.