FDA Inspection 1019264 — Busch Robert, M.D.

Busch Robert, M.D. — FEI 3008431791

The FDA completed an inspection of Busch Robert, M.D. on June 29, 2017 in Albany, NY. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 29, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Albany, NY (United States)

Additional Details

Clinical Investigator (CI)