FDA Inspection 1025631 — Stefano Bonarelli, M.D.

Stefano Bonarelli, M.D. — FEI 3013302141

The FDA completed an inspection of Stefano Bonarelli, M.D. on May 19, 2017 in Ior-Irccs, Bologna. 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). 3 citations were issued during this inspection. Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
May 19, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Ior-Irccs, Bologna (Italy)

Additional details

Clinical Investigator (CI)

Citations

IDCFRDescription
752021 CFR 312.64(b)Safety reports
753021 CFR 312.62(b)Case history records- inadequate or inadequate
756021 CFR 312.60FD-1572, protocol compliance

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