FDA Inspection 1070940 — Benjamin N. Lockshin, M.D.

Benjamin N. Lockshin, M.D. — FEI 3014774158

The FDA completed an inspection of Benjamin N. Lockshin, M.D. on Nov 1, 2018 in Rockville, MD. 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). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 1, 2018
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Rockville, MD (United States)

Additional Details

Clinical Investigator (CI)