FDA Inspection 1003397 — Rumen Stoilov, M.D.

Rumen Stoilov, M.D. — FEI 3013105237

The FDA completed an inspection of Rumen Stoilov, M.D. on Feb 9, 2017 in Sofia, Bulgaria. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Feb 9, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Sofia, Bulgaria (Bulgaria)

Additional Details

Clinical Investigator (CI)

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