FDA Inspection 1294054 — Amandeep Salhotra, M.D.

Amandeep Salhotra, M.D. — FEI 3030392265

The FDA completed an inspection of Amandeep Salhotra, M.D. on December 4, 2025 in Duarte, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 4, 2025
Fiscal Year
2026
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Duarte, CA (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
756021 CFR 312.60FD-1572, protocol compliance