FDA Inspection 1289504 — Dr. Manish Butte, M.D.

Dr. Manish Butte, M.D. — FEI 3039670956

The FDA completed an inspection of Dr. Manish Butte, M.D. on Oct 24, 2025 in Los Angeles, CA. 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
Oct 24, 2025
Fiscal Year
2026
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Los Angeles, CA (United States)

Additional Details

Clinical BA/BE

Citations

IDCFRDescription
2272821 CFR 312.64(b)Safety Reports - Non-Serious Events
753021 CFR 312.62(b)Case history records- inadequate or inadequate
756021 CFR 312.60FD-1572, protocol compliance

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